CURRICULUM VITAE

                                            June 24, 2005

                                      AHMAD S...
Cross Appointments

2003          Associate Staff, Division of Hematology/Oncology, University Health Network,
           ...
NATIONAL AND INTERNATIONAL AFFILIATIONS AND ACTIVITIES
Editorial Boards

2005          Member, Clinical Genetics
2004     ...
•   Medical Sciences Monitor
•   Pediatrics
•   Pediatric Research
•   Social Science and Medicine


Scientific Reviewer

...
1996 - 1998   Member, McGill Genetics Services integration committee, Montreal
1994 - 1998   Member, Medical Genetics Boar...
Genetics 1984: 20 (6): pp 464 - 465. CPA

8.    Al-Awadi SA, Farag TI, Naguib KK, Teebi AS, Cuschieri A. Youssef F, Hassan...
20.   Al-Awadi SA, Naguib KK, Farag TI, Teebi AS, Cuschieri A, Al-Othman SA,
      Sundareshan TS: Complex translocation i...
33.   Al-Awadi SA, Farag TI, Teebi AS, Naguib KK, El-Khalifa MY, Al-Fadalah S: Otologic
      abnormalities in 53 Arab Dow...
47.   AS Teebi, Al-Awadi SA, Marafie MJ, Bushnaq RA, Satyanath S: Osteoporosis-
      pseudoglioma syndrome with congenita...
62.   Awadalla NB, Teebi AS, El-Zouki A, Shaltout A: Frequent relapser minimal change
      nephrosis: An unrecognized X-l...
311-312. PA

76.   Teebi AS, Al-Saleh QA, Hassoon MM, Farag TI, Al-Awadi SA: Macrosomia,
      microphthalmia, cleft palat...
chromosome 2 (2q11) with unusual features and psychomotor retardation. Ind J Paediatr
       1990: 57: pp 257-260. C

90. ...
104.   Teebi AS, Kishawi A, Malek AH: Male triplets concordant for X-linked recessive
       nonsyndromic hypoparathyroidi...
117.   Teebi AS: Autosomal recessive disorders among Arabs. An overview from Kuwait (Invited
       article). Journal of M...
132.   * - Al-Ata J, M Paquet, Teebi AS: The Spectrum of congenital heart disease in Robinow
       syndrome. American Jou...
145.   Elliott AM, Teebi AS: New autosomal dominant syndrome reminiscent of Coffin-Siris
       syndrome and Brachymorphis...
157.   * - Clarkson B, Pavenski K, Dupuis L, Kennedy S, Meyn S, Nezarati M, Nie G,
       Weksberg R, Withers S, Quercia N...
168.   Teebi AS: Editorial: Medical Genetics and The Practitioner: Understanding the Language.
       Journal of the Islam...
180. * - Lemire BD, Kennedy SJ, Teebi AS: Congenital mydriasis, patent ductus arteriosus, and
        congenital cystic lu...
4. Teebi AS, Shawky R: Population and molecular genetic update: The second Middle East
   Genetics Association (MEGA) Conf...
TI, eds). Oxford University Press, New York, NY 1997: pp 474-486. CPA

8.    Farag TI, Teebi AS: Genetic Disorders among t...
Throat (Tewfik TL, Der Kaloustian VM, eds). Oxford University Press, NY 1997: pp
      393-400. CPA

20.   Tewfik TL, Teeb...
1-33. PA


Abstracts

1.    Al-Awadi SA, Farag TI, Naguib KK, Teebi AS: Six hemizygous male sibs with X-linked
      hydro...
Conference, Edinburgh. 1992: pp A2, 71. C

14.   Teebi AS, Gibson L, McGrath J, Meyn MS, Breg TL, Yang-Feng T: Molecular a...
26.   * - Kaurah P, Teebi AS: Total Anonychia congenita and microcephaly with normal
      intelligence in 2 siblings of c...
38.   Azouz EM, Teebi AS: New autosomal dominant rhizomesomelic short stature syndrome.
      American Journal of Human Ge...
48.   * - Chun KM, Teebi AS, Kennedy SJ, Forrest CR, Ray PN: Graduated strategy for the
      molecular diagnosis of crani...
60.   Teebi AS, Teebi SA, Porter C, Cuticchia AJ: Arab Genetic Database (AGDDB) Mutation
      Database Initiative. Americ...
73.   Teebi AS: Genetic databases. Conference in Child Health and the 9th Conference of the
      Union of Arab Pediatric ...
84.   Ul Haque MF, Teebi AS, Al-Ali M, Al-Mureikhi MS, Kennedy SJ, Al-Thani G, Zaidi
      SHE, Tsui L-C: A Novel Homozygo...
96.    Hamamy H, Ajlouni K, Teebi AS: Midface Prominence, Dental/Enamel Hypoplasia,
       Prominent/Simple Ears, Osteopen...
Rearrangement Between the Telomere of 7p and 20q Resulting in Partial Trisomy 20qter/Partial
     Monosomy 7pter: Clinical...
Sep 1991. The private syndrome.

7.    Alfred Dupont Institute & Nemours Children's Clinic, Pediatric Grand Rounds, Jackso...
23.   Pediatric Grand Rounds, Saskatoon, Saskatchewan, Sep 1996. What is dysmorphology and
      what dysmorphology does.
...
Establishing genetic services in a Gulf country.

40.   12th. International Child Health Conference, Muscat, Oman, Feb 199...
56.   King Faisal Specialist Hospital, Jeddah, Saudi Arabia, Apr 2001. Pediatric at a Glance
      Symposium. Genetic diso...
72.   American College of Medical Genetics, Annual Clinical Genetics Meeting, New Orleans,
      Louisiana, Mar 2002. Card...
88.    Kuwait Medical Genetic Center, Kuwait, Dec 17, 2002. Genetic Disease Profile Among The
       Arabs in Kuwait.

89....
Pediatric Grand Rounds. Neurodevelopment and Dysmorphology: Clues for Diagnosis.

105.   Society of Craniofacial Genetics,...
Ahmad Said Teebi, Canada.doc
Ahmad Said Teebi, Canada.doc
Ahmad Said Teebi, Canada.doc
Ahmad Said Teebi, Canada.doc
Ahmad Said Teebi, Canada.doc
Ahmad Said Teebi, Canada.doc
Ahmad Said Teebi, Canada.doc
Ahmad Said Teebi, Canada.doc
Ahmad Said Teebi, Canada.doc
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  1. 1. CURRICULUM VITAE June 24, 2005 AHMAD SAID TEEBI Hospital for Sick Children 555 University Avenue Toronto, ON Canada M5G 1X8 Telephone: (416) 813-6389, (416) 813-8366 Fax: (416) 813-5345 E-mail: ahmad.teebi@sickkids.ca EDUCATION 1967 – 1973 M.B., B.Ch., Cairo University Egypt 1976 – 1977 Diploma in Child Health, D.C.H., University College, Dublin, Ireland 1982 – 1983 Diploma in Human and Clinical Genetics, D.H.C.G., London School of Hygiene and Tropical Medicine, University of London, London, U.K. Certification: 2005 Fellow of the Royal College of Physicians of Canada (F.R.C.P.C.)- Medical Genetics 1997 Certificat de Specialiste College des M’edecins du Quebec (C.S.P.Q.). Medical Genetics 1996 Fellow of the Royal College of Physicians of Edinburgh (F.R.C.P.E.) - Pediatrics 1994 Fellow of the American College of Medical Genetics (F.A.C.M.G.) 1993 Board Certified - American Board of Medical Genetics (A.B.M.G. - Clinical Genetics) 1991 Board Eligible - A.B.M.G. 1991 ECFMG #2469519 Present Appointments: 2000 Head, Section of Clinical Genetics & Dysmorphology, Division of Clinical and Metabolic Genetics, The Hospital for Sick Children (HSC), Toronto 2000 Project Director, Research Institute, The Hospital for Sick Children 1999 Professor, Graduate Department of Molecular and Medical Genetics – School of Graduate Studies, University of Toronto 1998 Clinical Geneticist, HSC Centre for Craniofacial Care and Research, HSC, Toronto 1998 Director, Craniofacial and Cleft Lip and Palate Genetic Clinics, HSC, Toronto 1998 Clinical Geneticist, Division of Clinical and Metabolic Genetics, HSC, Toronto 1998 Professor, Department of Pediatrics, Department of Medical Genetics, and Microbiology, University of Toronto
  2. 2. Cross Appointments 2003 Associate Staff, Division of Hematology/Oncology, University Health Network, Toronto, ON 1999 Courtesy Staff, Pediatric Department, Mount Sinai Hospital, Toronto Past Appointments 2003 – 2004 Chairman, Department of Medical Geneticist, King Faisal Specialist and Research Center, Riyadh, Saudi Arabia (Sabbatical leave). 1993 – 1998 Associate Professor, Department of Pediatric and Human Genetics, McGill University 1993 – 1998 Clinical Geneticist, Montreal Children’s Hospital, Montreal, Quebec, Canada 1997 – 1998 Consultant Clinical Geneticist, Royal Victoria Hospital and Jewish General Hospital, Montreal 1992 – 1993 Instructor in Genetics and Pediatrics, Yale University School of Medicine, New Haven, CT, USA 1990 – 1993 Fellow in Genetics and Pediatrics, Yale Hospital, New Haven, CT, USA 1983 – 1990 Clinical Geneticist and Dysmorphologist, Kuwait Medical Genetics and Satellite Genetics Clinic at Amiri and Farwania Hospitals, Kuwait 01-/02/1986 Fellow in Medical Genetics, University of British Columbia Vancouver, Canada 1981- 1983 Geneticist in training (Registrar), Kuwait Medical Genetics Centre, Kuwait 1979 – 1981 Chief Resident in Pediatrics (Registrar) – Al-Sabah Teaching Hospital, Kuwait 1975 – 1979 Resident in Pediatrics, Al-Sabah Teaching Hospital, Kuwait 1974 – 1975 Rotating Internship, Cairo Univ. Hospitals, Egypt and Al-Sabah Teaching Hosp., Kuwait Awards and Honours 2004 Richard Rowe Award for Clinical Excellence. The Hospital for Sick Children (Runner up) 2002 Elected – member of European Academy of Sciences 2001 Rammal Award, Euroscience Foundation, given for recognition of both scientific achievement and commitment and the cause of Mediterranean cooperation. 1990 – 1993 NIH training & Research Award. Genetics Fellowship – Yale, New Haven, USA 1989 Kuwait Prize in Basic Science (Genetics), by Kuwait Foundation for Advancement of Science (KFAS), given for outstanding contribution in Clinical and Human Genetics in the Arab World. 1977 D.C.H. Silver Medal, Dublin & Kuwait 1968 – 1973 UNRWA Scholarship, Cairo, Egypt Medical Licensure 1998 Ontario, College of Physicians and Surgeons of Ontario #72147 (Academic). 1993 - 1998 Quebec, College de Médecins du Québec #93-330 (Restricted). 1975 - 1990 Kuwait, Ministry of Public Health #133/75 1975 Egypt
  3. 3. NATIONAL AND INTERNATIONAL AFFILIATIONS AND ACTIVITIES Editorial Boards 2005 Member, Clinical Genetics 2004 Member, National Genetic and Birth Defects Registry (NGBDR), Saudi Arabia 2004 Member, American Journal of Medical Genetics 2003 Guest Editor, JIMA Special Issue Clinical Genetics 2002 Member, JIMA 2002 Member, the Egyptian Journal of Human Medical Genetics 1999 - 2000 Section Editor (Genetics) of Textbook of Clinical Pediatrics [Editor: A. Elzouki], Lippincott, Williams & Wilkins, London 1997 Editor, Textbook: Genetic Disorders Among Arab Population. Oxford University Press, Oxford, NY. 1997 Member, Qatar Medical Journal 1995 Member, Gulf Journal of Dermatology 1991 - 1995 Member, Clinical Dysmorphology (Founding member, term membership) 1988 - 1990 Associate Editor, Journal of Kuwait Medical Association 1987 - 1988 Member, Journal of Kuwait Medical Association Other 1998 Arab Genetic Diseases Consortium (Foundation) 1999 Dysmorphology Group of Ontario 1999 Association of Genetics Colleagues of Ontario (AGCO) 1998 Ontario HHT network 1998 Ethnic & National databases working group – HUGO mutation database initiative 1998 Cornelia de Lange Syndrome Canada, Medical & Advisory Board 1997 Canadian Cancer Genetics Network 1996 – 2000 Middle East Genetics Association of America (MEGA) - President 1994 PAH Consortium. Journal Reviewer • Annals of Saudi Medicine • American Journal of Medical Genetics • Archives of Dermatological Research • Clinical Biochemistry • Clinical Genetics • Clinical Dysmorphology • Community Genetics • Genetic in Medicine • East Mediterranean Health Journal • Emirates Medical Journal • European Journal of Human Genetics • Human Biology • Human Mutation • J of Medical Genetics • J Otolaryngology • J Rheumatology • McGill Journal of Medicine (MJM)
  4. 4. • Medical Sciences Monitor • Pediatrics • Pediatric Research • Social Science and Medicine Scientific Reviewer • Oxford University Press (Book proposals) • Montreal Children’s Hospital Research Institute (Grants) • Hospital for Sick Children Research Institute, Internal Review Committee (Grants) • Faculty of Science, Cairo University (Ph.D. examiner) • Sultan Qaboos University, Oman (Grants) • Quaid-I-Azam University, Islamabad (Ph.D. examiner) Professional Society Memberships 2004 Member, European Society of Human Genetics 2000 Member, National Arab American Medical Association 1999 Member, Fetal Alcohol Canadian Expertise (FACE). The Hospital for Sick Children, Toronto, ON 1998 College of Physicians and Surgeons of Ontario 1997 - 2000 President, Middle-East Genetics Association (MEGA) 1997 - 1998 Federation des médecins specialistes du Québec 1997 - 1998 Association des médecins généticiens du Québec 1996 Founding member, Middle-East Genetics Association, USA, (MEGA). 1996 Royal College of Physicians, Edinburgh 1989 American Society of Human Genetics (ASHG) 1975 - 1990 Kuwait Medical Association 1982 - 1990 Clinical Genetics Society, U.K 1981 - 1990 The Society for the Study of Inborn Errors of Metabolism, U.K Professional Committees 2004 Diagnostic Code Committee, Division of Clinical & Metabolic Genetics, Hospital for Sick Children, Toronto, ON 2003 Medical Genetics. Post Graduate Education Committee, University of Toronto. 2000 Chair, Protocols Committee, Division of Clinical & Metabolic Genetics, Hospital for Sick Children, Toronto 1999 - 2000 Molecular Medicine Post-graduate Education Committee, University of Toronto, Toronto 1998 Fellows and Residents Supervisory Committees, Hospital for Sick Children and University of Toronto, Toronto 1998 Genetic Staff Search Committees, Division of Clinical & Metabolic Genetics, Hospital for Sick Children, Toronto 1998 Child Health Network Committee, Hospital for Sick Children, Toronto 1997 - 1998 Montreal Children’s Hospital Governor’s Circle Committee, Montreal 1997 - 1998 McGill Genetics Fellowship Training Committee, McGill University, Montreal 1997 - 1999 Organizing and scientific committees of the 2nd. MEGA Conference. Cairo, November 1999 1996 - 1997 Organizing and Scientific Committees of the Joint Symposium of Institut Pasteur de Tunis and MEGA, December 1997
  5. 5. 1996 - 1998 Member, McGill Genetics Services integration committee, Montreal 1994 - 1998 Member, Medical Genetics Board, Montreal Children's Hospital, Montreal 1994 - 1998 Member, Search Committee for Director of Medical Genetics, Montreal Children's Hospital /McGill University. 1992 - 1993 Member, Genetic Fellowship Educational Committee, Yale University, New Haven 1988 - 1990 Member, Educational Committee in Pediatrics, Kuwait Institute of Medical Specialties, Kuwait 1988 - 1990 Member, Scientific Committee, Kuwait Medical Association, Kuwait 1985 - 1987 Member, Ethical Committee, Kuwait Medical Association, Kuwait 1985 - 1990 Member, Task Force Committee for Inherited Metabolic Diseases, Kuwait 1984 - 1987 Member/Coordinator, Neonatal Screening Program for Metabolic Disease, Ministry of Health, Kuwait PUBLICATIONS PA-denotes Principal Author; SRI-Senior Responsible Investigator; CPA-Co-Principal Author; C-Collaborator Peer Reviewed - Journal Publications Published 1. Al-Awadi SA, Cuschieri A, Farag TI, Naguib KK, Teebi AS, Al-Othman SA, Bahig AH: Ullrich-Turner syndrome in monozygotic twins. American Journal of Medical Genetics 1983: 15: pp 537-542. C 2. Al-Awadi SA, Cuschieri A, Farag TI, Naguib KK, Teebi AS, Issa M, El-Sayed M: Mixed gonadal dysgenesis and sex chromosome mosaicism with multiple cell lines including structural aberrations of the Y chromosome. Clinical Genetics 1983: 23: pp 172-176. C 3. Al-Awadi SA, Farag TI, Cuschieri A, Naguib KK, Teebi AS: Autosomal recessive inheritance of intestinal atresia. Journal of the Royal Society of Medicine 1983: 76: pp 434-435. C 4. Al-Awadi SA, Farag TI, Naguib KK, Teebi AS, Cuschieri A, Al-Othman SA, Sundareshan TS: Interstitial deletion of the long arm of chromosome 2. Journal of Medical Genetics 1983: 20(6): pp 464-465. CPA 5. Al-Awadi SA, Farag TI, Naguib KK, Teebi AS, Cuschieri A, Youssef F, Hassan S: Bilateral total gonadectomy in Ullrich-Turner syndrome. Journal of Kuwait Medical Association 1983: 17: pp 242-244. C 6. Teebi AS: Primary hypomagnesemia: An X-borne allele? Lancet 1983: 1(8326): pp 701. PA 7. Al-Awadi SA, Farag TI, Naguib KK, Teebi AS, Cuschieri A, Al-Othman SA, Sundareshan TS: Interstitial deletion of the long arm of chromosome 2. Journal of Medical
  6. 6. Genetics 1984: 20 (6): pp 464 - 465. CPA 8. Al-Awadi SA, Farag TI, Naguib KK, Teebi AS, Cuschieri A. Youssef F, Hassan S: Bilateral total gonadectomy in Ullrich-Turner syndrome. J Kwt Med Assoc 1984: 17: pp 242 - 244. C 9. Al-Awadi SA, Farag TI, Naguib KK, Teebi AS, El-Khalifa MY, Al-Othman SA, Sundareshan TS: A five-year experience with gonosomal abnormalities in Kuwait. J Kwt Med Assoc 1984: 18: pp 225 - 232. CPA 10. Al-Awadi SA, Farag TI, Naguib KK, Teebi AS, El-Khalifa MY, S. Yassin: X-linked hydrocephalus (Bicker-Adams-Edwards syndrome). Journal of Kuwait Medical Association 1984: 18: pp 187-190. C 11. Al-Awadi SA, Farag TI, Teebi AS, Naguib KK, El-Khalifa MY: Anencephaly: Disappearing in Kuwait. Lancet 1984: 2(8404): pp 701-702. C 12. Al-Awadi SA, Farag TI, Teebi AS, Naguib KK, Aref MA, Badramany MH, El-Khorafy N, El-Kassaby TA: Tetrasomy X (48,XXXX syndrome). Journal of Kuwait Medical Association 1985: 19: pp 269-275. CPA 13. Al-Awadi SA, Farag TI, Teebi AS, Naguib KK, El-Khalifa MY, Kelani Y, Al-Ansari A: Hypergonadotropic hypogonadism with partial dysplasia of skin appendages. A new autosomal recessive syndrome. Saudi Med J 1985: 6: pp 355 - 360. CPA 14. Al-Awadi SA, Farag TI, Teebi AS, Naguib KK, El-Khalifa MY, Kelani Y, Al-Ansari A, Schimke RN: Primary hypogonadism and partial alopecia in three sibs with mullerian hypoplasia in the affected females. American Journal of Medical Genetics 1985: 22: pp 619 - 622. CPA 15. Al-Awadi SA, Moussa MA, Naguib KK, Farag TI, Teebi AS, El-Khalifa M, El-Dossary L: Consanguinity among the Kuwaiti population. Clinical Genetics 1985: 27: pp 483-486. CPA 16. Al-Awadi SA, Teebi AS, Farag TI, Naguib KK, El-Khalifa MY, Al-Othman SA, Sundareshan TS: A five-year experience with autosomal abnormalities in Kuwait. Journal of Kuwait Medical Association 1985: 19: pp 269-275. CPA 17. Al-Awadi SA, Teebi AS, Farag TI, Naguib KM, El-Khalifa MY: Profound limb deficiency, thoracic dystrophy, unusual facies and normal intelligence: A new syndrome. Journal of Medical Genetics 1985: 22: pp 36-38. PA 18. Al-Awadi SA, Teebi AS, Sundareshan TS: Complex chromosomal rearrangements involving chromosomes 11, 13, 14 and 18 resulting in monosomy for 13q32 qter. Ann Genet 1985: 28: pp 181-184. CPA 19. Tahan AM, Al-Khateeb WO, Teebi AS, Abu Jyab AK: HLA markers in IDDM and non- IDDM in the Kuwaiti population. Arab Journal of Medicine 1985: 4(11): pp 7-9. C
  7. 7. 20. Al-Awadi SA, Naguib KK, Farag TI, Teebi AS, Cuschieri A, Al-Othman SA, Sundareshan TS: Complex translocation involving Y, 1 and 3 resulting in deletion of segment 3q23 q25. Journal of Medical Genetics 1986: 23: pp 91-92. C 21. Al-Awadi SA, Naguib KK, Moussa MA, Farag TI, Teebi AS: Effect of consanguineous marriages on reproductive wastage. Clinical Genetics 1986: 29: pp 384-388. CPA 22. Al-Awadi SA, Naguib KK, Teebi AS, Farag TI, Devarajan LV, El-Khalifa MY: Lethal multiple pterygium syndrome: Report of 2 sporadic cases from Kuwait. Journal of Kuwait Medical Association 1986: 20: pp 135-140. CPA 23. Al-Awadi SA, Naguib KK, Teebi AS, Sundareshan TS: De novo partial monosomy 21 with unusual karyotype. Jpn Journal of Human Genetics 1986: 31: pp 45-48. CPA 24. Al-Awadi SA, Teebi AS, Krishna Murthy DS, Othman G, Sundareshan TS: Klinefelter's syndrome mosaic 46,XX/46,XY/47,XXY, /48,XXYY. Annals of Genetics 1986: 29: pp 119-121. CPA 25. Bessiso MS, Teebi AS, Al-Awadi SA, Al-Rashied AA: Schwartz Jampel syndrome. Journal of Kuwait Medical Association 1986: 20: pp 195-199. CPA 26. Farag TI, Teebi AS, Al-Awadi SA: Nonsyndromal anencephaly: possible autosomal recessive variant. American Journal of Medical Genetics 1986: 24: pp 461-464. PA 27. Naguib KK, Al-Awadi SA, Farag TI, Teebi AS, El-Khalifa MY, Devarajan LV, Shaath R: Amniotic band syndrome and fetal deformation. Journal of Kuwait Medical Association 1986: 20: pp 89-97. CPA 28. Teebi AS, Al-Awadi SA: Spondyloepiphyseal dysplasia tarda with progressive arthropathy: A rare disorder frequently diagnosed among Arabs. Journal of Medical Genetics 1986: 23: pp 189-191. PA 29. Teebi AS, Al-Awadi SA, Farag TI, Naguib KK: Hypogonadotropic hypogonadism, mental retardation, obesity and minor skeletal abnormalities: Another new autosomal recessive syndrome from the Middle East. American Journal of Medical Genetics 1986: 24: pp 373-378. PA 30. Teebi AS, Al-Awadi SA, Opitz JM, Spranger J: Severe short limb dwarfism resembling Grebe chondrodysplasia. Human Genetics 1986: 74: pp 386-390. PA 31. Al-Awadi SA, Farag TI, Naguib KK, Teebi AS, El-Khalifa MY: Intestinal malformation and Down's syndrome in the Arabs. Journal of the Royal Society of Medicine 1987: 80: pp 61-62. CPA 32. Al-Awadi SA, Farag TI, Teebi AS, Naguib KK, Al-Othman SA, Sundareshan TS, Krishna Murthy DS: Down syndrome in Kuwait: Cytogenetic profile in 635 cases and comparative study with worldwide surveys. Journal of Kuwait Medical Association 1987: 21: pp 191-196. CPA
  8. 8. 33. Al-Awadi SA, Farag TI, Teebi AS, Naguib KK, El-Khalifa MY, Al-Fadalah S: Otologic abnormalities in 53 Arab Down's syndrome children. Journal of Kuwait Medical Association 1987: 21: pp 342-343. CPA 34. Al-Awadi SA, Naguib KK, Farag TI, Teebi AS: Hypoplastic tibiae and postaxial polysyndactyly: A new dominant syndrome? Journal of Medical Genetics 1987: 21: pp 328-330. CPA 35. Dudin KI, Teebi AS: Primary hypomagnesemia. A case report and literature review. European Journal of Pediatrics 1987: 146: pp 203-205. PA 36. Farag TI, Teebi AS, Naguib KK, El-Khalifa MY, Marafie MJ, Sundareshan TS, Al- Othman AA, Al-Awadi SA: Cytogenetic profile of Klinefelter syndrome in Kuwait. Journal of Kuwait Medical Association 1987: 21: pp 299-303. CPA 37. Mahfouz EH, Issa MA, Farag TI, Naguib KK, Teebi AS, El-Khalifa MY, Al-Awadi SA: Down syndrome and intestinal malformations in Kuwait. Journal of Kuwait Medical Association 1987: 21: pp 197-200. CPA 38. Naguib KK, Teebi AS, Al-Awadi SA, Marafie MJ: Brachmann-de Lange in sibs. Journal of Med Genet 1987: 24: pp 627-629. PA 39. Naguib KK, Teebi AS, Al-Awadi SA, Moosa A, Ali NR: Multiple pterygium syndrome in five Arab sibs. Annals of Genetics 1987: 30: pp 122-125. CPA 40. Portoian- Shuhaiber S, Jumaa K, Hamlawi H, Malla OK, Teebi AS, Al-Rashied AA: Siblings with a progressive neurodegenerative condition associated with basal ganglia calcifications, retinitis pigmentosa and decreased levels of fucosidase: a new presentation? Journal of Inherited Metabolic Diseases 1987: 10: pp 397-398. C 41. Shaath RI, Teebi AS, Al-Rashied AA: Thoracic ectopia cordis. Journal of Kuwait Medical Association 1987: 21: pp 328-330. CPA 42. Shuhaiber SP, Wright D, Teebi AS: How far to investigate a case of cerebral palsy. Saudi Medical Journal 1987: 8: pp 534-535. PA 43. Teebi AS: New autosomal dominant syndrome resembling craniofrontonasal dysplasia. American Journal of Medical Genetics 1987: 28: pp 581-591. PA 44. Teebi AS, Al-Awadi SA, Farag TI, Naguib KK, El-Khalifa MY: Phenylketonuria in Kuwait and Arab countries. European Journal of Pediatrics 1987: 146: pp 59-60. PA 45. Teebi AS, Al-Awadi SA, White AG: Autosomal recessive nonsyndromal microcephaly with normal intelligence. American Journal of Medical Genetics 1987: 26: pp 355-359. PA 46. Al-Awadi SA, Farag TI, Teebi AS, Naguib KK, Sundareshan TS, Ramadan AA, Krishna Murthy DS: Robertsonian translocations and their clinical implications: A study of 35 cases. Journal of Kuwait Medical Association 1988: 22: pp 263-268. CPA
  9. 9. 47. AS Teebi, Al-Awadi SA, Marafie MJ, Bushnaq RA, Satyanath S: Osteoporosis- pseudoglioma syndrome with congenital heart disease: A new association. Journal of Medical Genetics 1988: 25: pp 32-36. PA 48. Eeg-Olofsson O, Al-Zuhair A, Teebi AS, Al-Essa MA: Abnormal mitochondria in the Rett syndrome. Brain Dev 1988: 10: pp 260-262. CPA 49. Farag TI, Teebi AS: A possible evidence of genetic predisposition to nondisjunction in man. Journal of Medical Genetics 1988: 25: pp 136-137. PA 50. Farag TI, Teebi AS: Bardet-Biedl and Laurence-Moon syndromes in a mixed Arab population. Clinical Genetics 1988: 33: pp 78-82. PA 51. Issa ARA, Teebi AS, Issa MA, Ahmad MS, Voncina D, Al-Rashied AA: Familial erythrophagocytic lymphohistiocytosis. Annals Saudi Med 1988: 8: pp 56-60. CPA 52. Issa ARA, Teebi AS, Issa MA, Shabani IS, Ramadan DJ: Metabolic alkalosis in cystic fibrosis: Atypical presentation in Kuwait. Ann Trop Pediatr 1988: 8: pp 271-272. C 53. Issa ARA, Yadav G, Teebi AS: Intrafamilial variability in citrullinemia. Journal of Inherited Metab Dis 1988: 11: pp 306-307. CPA 54. Naguib KK, Al-Awadi SA, Teebi AS, Farag TI, Mowafi R, Marafie MJ, Ramadan AA: Holoprosencephaly in Kuwait: A study of 13 cases and literature review. Journal of Kuwait Medical Association 1988: 22: pp 41-47. CPA 55. Teebi AS: Neonatal screening for inherited metabolic disease: The need for introducing a new service in Kuwait (Editorial). Journal of Kuwait Medical Association 1988: 22: pp 197. PA 56. Teebi AS, Marafie MJ: Uncle-Niece/Aunt-Nephew marriages are not existing among Arab Muslims. American Journal of Medical Genetics 1988: 30: pp 981. PA 57. Teebi AS, Naguib KK: Autosomal recessive nonsyndromal hydrocephalus. American Journal Med Genet 1988: 31: pp 467-470. PA 58. Teebi AS, Naguib KK, Al-Awadi SA, Al-Saleh QA: New autosomal recessive faciodigitogenital syndrome. Journal of Medical Genetics 1988: 25: pp 400-406. PA 59. * - Kishawi A, Malik AH, Al-Awadi SA, Teebi AS: Hallermann-Streiff syndrome. Journal of Kuwait Medical Association 1989: 23: pp 80-81. SRI 60. Al-Awadi SA, Farag TI, Teebi AS, Naguib KK, Sundareshan TS, Murthy DS: Down syndrome in Kuwait. American Journal of Medical Genetics Suppl 1989: 7: pp 87 - 88. C 61. Al-Awadi SA, Sundareshan TS, Teebi AS, Hashash N, Abu Al-Assad FM, Aboo-Backer KC: Distal 10q trisomy: A clinically recognizable syndrome. Med Princ Pract 1989: 1: pp 112-114. CPA
  10. 10. 62. Awadalla NB, Teebi AS, El-Zouki A, Shaltout A: Frequent relapser minimal change nephrosis: An unrecognized X-linked disorder. European Journal of Pediatr 1989: 149: pp 205-207. CPA 63. Daoud AS, Zaki M, Al-Saleh QA, Teebi AS, Al-Awadi SA: Congenital hypothyroidism in Kuwait. Journal of Trop Paediatr 1989: 35: pp 312-314. CPA 64. Eeg-Olofsson O, Al-Zuhair A, Teebi AS, Al-Essa MA: Rett syndrome: Genetic clues based on mitochondrial changes in muscle. American Journal of Med Genet 1989: 32: pp 142-144. CPA 65. Farag TI, Kelani YAZ, Teebi AS, Naguib KK, Sundareshan TS, Al-Awadi SA, El- Khalifa MY, Marafie MJ, Bastaki L, Al-Othman SA: Clustering of major chromosomal abnormalities among unselected sterile men in Kuwait. Med Princ Pract 1989: 1: pp 232-235. CPA 66. Farag TI, Teebi AS: Apple-peel syndrome in sibs. Journal of Med Genet 1989: 26: pp 67-68. CPA 67. Farag TI, Teebi AS: High incidence of Bardet-Biedl syndrome among the Bedouins. Clinical Genetics 1989: 36: pp 463-465. PA 68. Farag TI, Teebi AS, Al-Awadi SA, El-Ramly M: Monozygotic twins concordant for Bardet-Biedl and benign acanthosis nigricans. Med Princ Pract 1989: 1: pp 60-62. CPA 69. Issa ARA, Wright DL, Tahboob SA, Teebi AS: Fatal Fulminant hepatitis in Wilson's disease: Report of two cases. Ann Saudi Med 1989: 9(6): pp 605-608. SRI 70. Majeed HA, Malak Kalaawi, Monhanty D, Teebi AS, Tunjekar MF, Al-Gharbawy F, Majeed SA, Al-Gazzar AH: Congenital dyserythropoietic anemia and chronic recurrent multifocal osteomyelitis in three related children and the association with sweet syndrome in two siblings. Pediatrics 1989: 115(5)Pt 1: pp 730-734. CPA 71. Naguib KK, Al-Awadi SA, Farag TI, Teebi AS, El-Alfi A, Marafie M, Al-Abood H: Syndromal and nonsyndromal cleft lip and cleft palate in Kuwait: A study of 166 cases. Ann Saudi Med 1989: 9: pp 388-392. CPA 72. Naguib KK, Al-Awadi SA, Mousa MAA, Farag TI, Teebi AS: Effect of paternal age, birth order and consanguinity on nondisjunction in the population of Kuwait. Journal of Kuwait Medical Association 1989: 23: pp 37-43. CPA 73. Naguib KK, Teebi AS, Farag TI, El-Khalifa MY, Al-Awadi SA, Mahfouz E: Familial uterine hernia syndrome: Report of a family with 4 affected males. American Journal of Med Genet 1989: 33: pp 180-181. CPA 74. Teebi AS, Al-Saleh QA: Autosomal dominant sneezing disorder provoked by fullness of stomach. Journal of Med Genet 1989: 26: pp 539-540. PA 75. Teebi AS, Al-Saleh QA: Nonsyndromal microphthalmia. Clinical Genetics 1989: 35: pp
  11. 11. 311-312. PA 76. Teebi AS, Al-Saleh QA, Hassoon MM, Farag TI, Al-Awadi SA: Macrosomia, microphthalmia, cleft palate, and early infant death: A new autosomal recessive syndrome. Clinical Genetics 1989: 36: pp 174-177. PA 77. Teebi AS, Farag TI: Macrosomia, microphthalmia and early rapid or sudden infant death: new syndrome? Pediatrics 1989: 83(4)S: pp 647-648. PA 78. Teebi AS, Farag TI, Bessiso MS: Urofacial syndrome. American Journal of Med Genet 1989: 34: pp 608. PA 79. Teebi AS, Krishna Murthy DS, Sundareshan TS, Al-Awadi SA, Jeryan LA, Baidas G, Dahouk W: Structural abnormalities of Y chromosome associated with infertility, short stature and hypospadias. Ann Saudi Med 1989: 9: pp 414-416. PA 80. Teebi AS, Shaltout A: New syndrome: Craniofacial anomalies, abnormal hair, camptodactyly and caudal appendage. American Journal of Med Genet 1989: 33(1): pp 58-60. PA 81. Teebi AS, Sundareshan TS, Hammouri MY, Al-Awadi SA, Al-Saleh QA: A new autosomal recessive disorder resembling Weaver syndrome. American Journal of Med Genet 1989: 33: pp 470-482. PA 82. * - Abulhasan SJ, Teebi AS, Zaki M, Hammad I, Al-Awadi SA, Krishna Murthy DS: Mosaicism 45,X/46,Xt dic (Xp;Xp) in a girl with short stature. Ann Genet 1990: 33: pp 234-238. CPA 83. Al-Saleh QA, Teebi AS: Autosomal recessive epidermolytic palmoplanter keratoderma. Journal of Med Genet 1990: 27: pp 519-522. PA 84. Eeg-Olofsson O, Al-Zuhair A, Teebi AS: A boy with Rett syndrome. Brain Dev 1990: 12: pp 529-532. CPA 85. Eeg-Olofsson O, Al-Zuhair A, Teebi AS, Daoud AS, Zaki M, Bessiso MS, Al-Essa MM: Rett syndrome: A mitochondrial disease? Journal of Child Neurology 1990: 5: pp 210-214. CPA 86. Farag TI, Teebi AS: Autosomal recessive inheritance of syndrome of hypertelorism, hypospadias, and Tetralogy of Fallot? American Journal of Med Genet 1990: 35: pp 516-518. PA 87. Farag TI, Teebi AS: Duchenne-like muscular dystrophy among Arabs. American Journal of Med Genet 1990: 37: pp 290. PA 88. Farag TI, Teebi AS: The second family of Spahr type metaphyseal chondrodysplasia: Autosomal recessive inheritance confirmed. Clin Genet 1990: 38: pp 237-239. PA 89. Krishna Murthy DS, Teebi AS, Al-Awadi SA: Familial fragile secondary constriction on
  12. 12. chromosome 2 (2q11) with unusual features and psychomotor retardation. Ind J Paediatr 1990: 57: pp 257-260. C 90. M. Lubani, Issa ARA, Bushnaq R, Al-Saleh QA, Dudin KI, Reavey PC, El-Khalifa MY, Manandhar DS, Abdul Al YK, Ismail EA, Teebi AS: Prevalence of congenital adrenal hyperplasia in Kuwait. European Journal of Pediatrics 1990: 149: pp 391-392. C 91. Teebi AS: Autosomal recessive Robinow syndrome. American Journal of Med Genet 1990: 35: pp 64-68. PA 92. Teebi AS: Mendelising inborn errors of morphogenesis. An overview from Kuwait. Journal of Kuwait Medical Association 1990: 24: pp 122-124. SRI 93. Teebi AS, Daoud AS: Multiple pterygium syndrome: a relatively common disorders among the Arabs. Journal of Med Genet 1990: 27: pp 791. PA 94. Zaki M, Teebi AS, Van der Meulen: Syndrome of renal tubular acidosis and sensorineural deafness: An intrafamilial variability. Med Princ Pract 1990: 2: pp 62-64. CPA 95. Hegab S, Sheriff SM, Naguib KK, Teebi AS, C.I. Phillips: Central Pulverulent (Coppock) Cataracts. A sibship of two Arab females with full-cousin parents. Opthalmic Pediatric Genet 1991: 12: pp 111-114. C 96. Lubani MM, Al-Saleh QA, Teebi AS, Moosa A, Kalawi MH: Cystic fibrosis and helicobacter pylori gastritis, megaloblastic anemia, subnormal mentality and minor anomalies in two siblings. A new syndrome? European Journal of Pediatrics 1991: 150: pp 253-255. CPA 97. Teebi AS: Trigonobrachycephaly, bulbous bifid nose, macrostomia, micrognathia, acral anomalies and hypotonia: A new autosomal recessive MCA/MR syndrome. American Journal of Med Genet 1991: 38: pp 529-531. PA 98. Teebi AS, Al-Awadi SA: Kuwait type faciodigitogenital syndrome. Journal of Med Genet 1991: 28: pp 805-808. PA 99. Teebi AS, Hassoon MM: Urofacial syndrome associated with hydrocephalus due to aqueductal stenosis. American Journal of Med Genet 1991: 40: pp 199-200. PA 100. * - Boles R, Teebi AS, Meyn MS: Pseudotrisomy 13 with bilateral limb shortness and radial hypoplasia. American Journal of Med Genet 1992: 44: pp 638-640. CPA 101. Teebi AS: Autosomal recessive Silver-Russell syndrome. Clin Dysmorphol 1992: 3: pp 151-156. PA 102. Teebi AS: Naguib-Richieri-Costa syndrome (Hypertelorism-hypospadias-polysyndactyly syndrome. American Journal of Med Genet 1992: 44: pp 115-116. PA 103. Teebi AS, Al-Saleh QA, Odeh H: Meckel syndrome and neural tube defects in Kuwait regional hospital. Journal of Med Genet 1992: 29: pp 140. PA
  13. 13. 104. Teebi AS, Kishawi A, Malek AH: Male triplets concordant for X-linked recessive nonsyndromic hypoparathyroidism. European Journal of Pediatrics 1992: 151(6): pp 468. PA 105. Teebi AS, Murthy DS, Ismail EA, Redha AA: Alagille syndrome and del (20)(p11.2). American Journal of Med Genet 1992: 42: pp 35-38. PA 106. Farag TI, Al-Awadi SA, El-Khalifa MY, Teebi AS, Naguib KK, El-Badramany MH: True and pseudo hermaphroditism: A decade of experience in Kuwait. Med Princ Pract 1993: 3: pp 156-159. C 107. * - Kogekar N, Teebi AS, Vockley J: Sandrow syndrome of mirror hands and feet and peculiar facies. American Journal of Med Genet 1993: 46: pp 126-128. SRI 108. Teebi AS: Costello syndrome or facio-cutaneous-skeletal syndrome. American Journal of Med Genet 1993: 47: pp 172. PA 109. Teebi AS: Limb/pelvis/uterus-hypoplasia/aplasia syndrome. Journal of Med Genet 1993: 30: pp 397. PA 110. Teebi AS, Gibson L, McGrath JM, Meyn MS, Breg R, Yang-Feng T: Molecular and Cytogenetic characterization of 9 p- anomalies. American Journal of Med Genet 1993: 46: pp 288-293. PA 111. Teebi AS, Rucquoi J, Meyn MS: Aarskog syndrome: Report of a family with review and discussion of nosology. American Journal of Med Genet 1993: 46: pp 501-509. PA 112. Teebi AS, Shabani IS: Further delineation of Costello Syndrome. American Journal of Med Genet 1993: 47: pp 166-168. PA 113. * - Boles R, Teebi AS, Schwartz D, Harper JF: Further delineation of the ear, patella, short stature syndrome (Meier-Gorlin syndrome). Clin Dysmorphol 1994: 3: pp 207-214. CPA 114. * - Chu TW, Teebi AS, Gibson L, Breg TL, Yang-Feng TL: FISH Diagnosis of partial trisomy 13 and tetrasomy 13 in a patient with severe trigonocephaly phenotype. American Journal of Med Genet 1994: 52: pp 92-96. SRI 115. * - Narayan D, Krishnan SN, Bhatt M, Ravikumar T, Mahoney MJ, Dolan TF, Haddad GG, Teebi AS: Unusual inheritance of Primary ciliary dyskinesia (Kartagener's syndrome). Journal of Med Genet 1994: 31: pp 493-496. SRI 116. Bender C, Buchler A, Schmidt-Mader B, Schlotter M, Teebi AS, Konecki DS, Trefz FK: Haplotype analysis and a new Msp1-polymorphism at the phenylalnine hydroxylase gene in the Arabian population. European Journal of Pediatrics 1994: 153(5). C
  14. 14. 117. Teebi AS: Autosomal recessive disorders among Arabs. An overview from Kuwait (Invited article). Journal of Med Genet 1994: 31: pp 224-233. PA 118. * - Bell M, Teebi AS: An autosomal dominant idiopathic scoliosis? American Journal of Med Genet 1995: 55: pp 112. SRI 119. Elliott A, Chen MF, Azouz M, Teebi AS: Developmental anomalies suggestive of the human homologue of the mouse disorganization mutant. American Journal of Med Genet 1995: 55: pp 240-243. SRI 120. Teebi AS, Ment L, Seashore M: Features of neurofibromatosis - Noonan Syndrome associated with moyamoya disease and tetralogy of Fallot. Gulf Journal of Dermatology 1995: 2: pp 52-55. PA 121. Teebi AS, Qumsiyeh MB, Meyers-Seifer GH, Meyn MS: Velo-facio-skeletal syndrome in a mother and daughter. American Journal of Med Genet 1995: 58: pp 8-12. PA 122. * - Hoodfar E, Teebi AS: Genetic referrals of Middle Eastern Origin in a Western City: Inbreeding and Disease Profile. Journal of Med Genet 1996: 33: pp 212-215. SRI 123. * - S Al-Fifi, Teebi AS, Shevell M: Autosomal dominant inheritance of Russell-Silver Syndrome. American Journal of Med Genet 1996: 61: pp 96-97. SRI 124. * - Teebi AS, Kaurah P: Total anonychia congenita and microcephaly with normal intelligence: A new autosomal recessive syndrome? American Journal of Med Genet 1996: 66: pp 257-260. PA 125. Elliott A, Ludman M, Teebi AS: New MCA/MR syndrome with circumferential skin creases. American Journal of Med Genet 1996: 62: pp 23-25. SRI 126. Teebi AS: Medical Genetics: Present and future. QMJ 1996: 6(1): pp 3-6. PA 127. Teebi AS, Elliott A: Another case of the human homologue of the mouse mutant disorganization. American Journal of Med Genet 1996: 61: pp 94. PA 128. * - Al-Ghamdi M, Polomeno R, Chitayat D, Azouz EM, Teebi AS: Arthrogryposis multiplex congenita, craniofacial and ophthalmological abnormalities and normal intelligence: A new syndrome? American Journal of Med Genet 1997: 71: pp 401-405. SRI 129. Elliott AM, Teebi AS: Further examples of autosomal dominant inheritance of cutis aplasia congenita. American Journal of Med Genet 1997: 73: pp 495-496. SRI 130. Fraser FC, Teebi AS, Walsh S, Pinsky L: Poland sequence with dextrocardia: Which comes first? American Journal of Med Genet 1997: 73: pp 194-196. CPA 131. Teebi AS, Gorlin RJ: Not a new Seckel-like syndrome but ear-patella-short stature syndrome. American Journal of Med Genet 1997: 70: pp 454. PA
  15. 15. 132. * - Al-Ata J, M Paquet, Teebi AS: The Spectrum of congenital heart disease in Robinow syndrome. American Journal of Med Genet 1998: 77: pp 332-333. SRI 133. * - Noreau DR, Al-Ata J, Jutras L, Teebi AS: Congenital Heart Disease in Sotos Syndrome. American Journal of Med Genet 1998: 79: pp 327-328. SRI 134. Azouz EM, Teebi AS, Eydoux P, Chen M-F, Fassier F: Bone dysplasias, an introduction. Canadian Assoc Radiol Journal 1998: 49: pp 105-109. CPA 135. Carethers JM, Furnari FB, Zigman AF, Lavine JE, Jones MC. Graham GE, Teebi AS, Su Huang HJ, Ha HT, Chauhan DP, Chang CL, Cavenee WK, Boland CR: Absence of TEN/MMACI Germ-line mutations in sporadic Bannayan - Riley - Ruvalcaba syndrome. Cancer Research 1998: 58: pp 2724-2726. C 136. Massoud AA, Ammaari AM, Khan ASS, Ven Katraman B, Teebi AS: Bartsocas-Papas syndrome in an Arab family with 4 affected siblings: Further characterization. American Journal of Med Genet 1998: 79: pp 16-21. SRI 137. Robb L, Teebi AS: Further evidence of autosomal dominant inheritance of the nonsyndromal anorectal malformations. American Journal of Med Genet 1998: 79: pp 400. SRI 138. Teebi AS, Lambert DM, Kaye G, Al-Fifi S, Tewfik TL, Azouz EM: Keutel syndrome: further characterization and review. American Journal of Med Genet 1998: 78: pp 182-187. PA 139. Teebi AS, Miller S, Ostrer H, Eydoux P, Watters G: Spastic paraplegia, optic atrophy, microcephaly with normal intelligence and XY sex reversal: A new autosomal recessive syndrome? Journal of Med Genet 1998: 35: pp 759-762. PA 140. * - Lemyre E, Azouz EM, Teebi AS: Achondroplasia, hypochondroplasia and thanatophoric dysplasia: Review and update. Canadian Association of Radiology Journal 1999: 50: pp 185-197. SRI 141. Elliott A, Graham G, Bernstein M, Mazer B, Teebi AS: Dyskeratosis Congenita: An autosomal recessive entity. American Journal of Medical Genetics 1999: 83: pp 178-182. SRI 142. * - Yoskovitch A, Tewfik TL, Nguyen L, Oudjhane K, Teebi AS: Choanal and ileal atresia: A new syndrome or association? International Journal of Pediatric Otorhinolaryngology 1999: 49: pp 237-240. SRI 143. Kennedy SJ, Lee KJ, McCrindle BW, Teebi AS: Microcephaly-cardiomyopathy syndrome: confirmation of the phenotype. Journal of Medical Genetics 1999: 36(11): pp 854-855. SRI 144. * - Chan AKJ, Levin A, Teebi AS: New case with craniofacial dysmorphism, agenesis of corpus callosum, and ocular colobomas: Temtamy syndrome? Clinical Dysmorphology 2000: 9: pp 223-226. SRI
  16. 16. 145. Elliott AM, Teebi AS: New autosomal dominant syndrome reminiscent of Coffin-Siris syndrome and Brachymorphism-Onychodysplasia-Dysphalangism syndrome. Clinical Dysmorphology 2000: 9(1): pp 15-19. PA 146. Teebi AS: Hypoparathyroidism, retarded growth and development, and dysmorphism or Sanjad-Sakati syndrome: An Arab disease reminiscent to Kenny-Caffey syndrome. Journal of Medical Genetics 2000: 37: pp 145. PA 147. * - Al-Sannaa N, Adatia I, Teebi AS: Transverse limb associated with aorto-pulmonary vascular abnormalities: vascular disruption sequence or atypical presentation of Adams- Oliver syndrome? American Journal of Medical Genetics 2000: 94: pp 400-404. SRI 148. Teebi AS: Nablus mask-like facial syndrome. American Journal of Medical Genetics 2000: 95 (4): pp 407-408. PA 149. * - Al-Khenaizan S, Al-Sannaa N, Teebi AS: What syndrome is this? Chondroectodermal dysplasia -- The Ellis-van Creveld syndrome. Pediatric Dermatology 2001: 18: pp 68-70. SRI 150. Teebi AS, Druker HA: Brachycephaly, cutis aplasia congenita, blue sclerae, hypertelorism, polydactyly, hypoplastic nipples, failure to thrive and developmental delay: a distinct autosomal recessive syndrome? Clinical Dysmorphology 2001: 10: pp 69-70. SRI 151. Teebi AS, Elliott A, Azouz EM, Lachman RS: Progressive erosive arthropathy with contractures, multicentric osteolysis-like changes, characteristic craniofacial appearance and dermatological abnormalities: a new syndrome? American Journal of Medical Genetics 2001: 100 (3): pp 198 - 203. PA 152. Teebi AS: Not new variant of the autosomal recessive multiple pterygium syndrome but the Bartsocas-Papas syndrome. American Journal of Medical Genetics 2001: 101 (1): pp 78 - 9. PA 153. * - Al-Sannaa N, Forrest CR, Teebi AS: Trigonomicrocephaly, severe micrognathia, large ears, atrioventricular septal defects, symmetrical cutaneous syndactyly of hands and feet, and multiple cafe-au-lait spots: anew acrocraniofacial dysostosis syndrome? American Journal of Medical Genetics 2001: 101 (3): pp 279 - 82. CPA 154. Kennedy SJ, Adatia I, Teshima I, Teebi AS: An Inherited Duplication, Dup (8) (pg23,1P23.1) Pat in a Father and Daughter with Congenital Heart Defects. American Journal of Medical Genetics 2001: 104 (1): pp 79-80. SRI 155. Quercia N, Teebi AS: Craniosynostosis, ectopia lentis, and congenital heart defects: Further delineation of an autosomal dominant syndrome with incomplete penetrance. American Journal of Medical Genetics 2002: 107 (1): pp 38 -42. SRI 156. Teebi AS, Kennedy S, Chun K, Ray PN: Severe and mild phenotypes in Pfeiffer Syndrome with splice acceptor: Report of two novel mutations in exon IIIc of FGFR2. American Journal of Medical Genetics 2002: 107 (1): pp 43 -47. CPA
  17. 17. 157. * - Clarkson B, Pavenski K, Dupuis L, Kennedy S, Meyn S, Nezarati M, Nie G, Weksberg R, Withers S, Quercia N, Teebi AS, Teshima I: Detecting Rearrangements in Children Using Subtelomeric FISH and SKY. American Journal of Medical Genetics 2002: 107: pp 267-274. CPA 158. Boerkoel CF, Takashima H, Garcia CA, Olney RK, Johnson J, Berry K, Russo P, Kennedy S, Teebi AS, Scavina M, Williams LL, Mancias P, Butler IJ, Krajewski K, Shy M, Lupski JR: Charcot-Marie-Tooth disease and related neuropathies: Mutation distribution and genotype-phenotype correlation. Ann Neurol 2002: 51(2): pp 190-201. C 159. Siegel-Bartelt J. Levin A, Kennedy SJ, Teebi AS: Craniofacial anomalies, cataracts, congenital heart disease, sacral neural tube defects, growth and developmental retardation in two sisters: A new MCA/MR syndrome. Journal of Medical Genetics 2002: 39(2): pp 145-8. SRI 160. * - Chun K, Teebi AS, Jung JH, Laframboise R, Nakabayashi K, Scherer SW, Ray PN, Teshima I: Genetic Analysis of Patients with the Saethre-Chotzen Phenotype. American Journal of Medical Genetics 2002: 110: pp 136-143. CPA 161. Faiyaz-Ul-Haque Muhammad, Ahmad Wasim, Zaidi Syed H. E, Haque Sayedul, Teebi AS, Ahmad Mahmud, Cohn Daniel H, and Tsui Lap-Chee: Mutation in the Cartilage Derived Morphogenetic Protein-1 (CDMP1) gene in a kindred affected with Fibular hypoplasia and Complex Brachydactyly (DuPan Syndrome). Clinical Genetics 2002: 61: pp 454-458. C 162. Teebi AS, Teebi SA, Porter C, Cuticchia J: Arab Genetic Diseases DataBase (AGDDB): A population specific clinical and mutation database. Human Mutation 2002: 19: pp 615-621. PA 163. Faiyaz-Ul-Haque M, Ahmad W, Abdul Wahab, Haque S, Azimi AC, Zaidi SHE, Teebi AS, Ahmad M, Cohn DH, Siddique T, Tsui L-C: A frame shift mutation induced premature termination of cartilage derived morphogenetic protein - 1 causes severe short limb dwarfism. American Journal of Medical Genetics 2002: 111: pp 31-37. C 164. Tsai Chun-Huii, Roberson J. R, Teebi AS: Teebi Hypertelorism Syndrome: Report of A Family With Previously Unrecognized Findings. American Journal of Medical Genetics 2002: 113(3): pp 302-6. C 165. *Azimi C, Kennedy S, Chitayat D, Chakraborty P, Clarke J, Forrest C, Teebi AS: Clinical and Genetic Aspects of Trigonocephaly: A Study of 25 Cases. American Journal of Medical Genetics 2003: 117A: pp 127-135. PA 166. Abdul Wahab A, Janahi IA, Ul Haque F, El-Tohami A, Zaid A, Chee Tsui L, Teebi AS: A New type of Ehlers-Danlos Syndrome Associated with Tortuous Systemic Arteries in a Large kindred from Qatar. Acta Pediatrica Scandanavica 2003: 92 (4): pp 456-462. CPA 167. Teebi AS: An Approach to Dysmorphology. JIMA 2003: 35: pp 6-6. PA
  18. 18. 168. Teebi AS: Editorial: Medical Genetics and The Practitioner: Understanding the Language. Journal of the Islamic Medical Association of North America 2003: 35: pp 5. PA 169. Scherer SW, Cheung J, MacDonald JR, Osborne LR, Nakabayashi K, ..........Teebi AS.......et.al: Human Chromosome 7 - DNA Sequence and Biology. Science 2003: 300: pp 685-848. C 170. * - Chun K, Azimi C, Teebi AS, Steele L, Ray PN: Screening of patients with craniosynostosis syndromes: Molecular strategy. American Journal of Medical Genetics (CPA) 2003: 120A(4): pp 470-3. CPA 171. * - Lo B, Ul-Haque FM Kennedy S, Teebi AS: Novel Mutation in the Gene Encoding c- Abl-binding Protein SH3BP2 Causes Cherubism. American Journal of Medical Genetics 2003: 121A(1): pp 37-40. SRI 172. Dowling O, Difeo A, Ramirez MC, Tukel T, Narla G, Bonafe L, Kayserili H, Yuksel- Apak M, Paller AS, Norton K, Grum-Tokars V, Martin GS, Davis, GE, Glucksman MJ, Teebi AS, Martignetti JA: Mutations in Capillary Morphogenesis Gene-2 Result in the Allelic Disorders Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis. American Journal of Human Genetics 2003: 73 (3): pp 957-66. C 173. * - Lo B, Faiyaz-Ul-Haque Muhammad, Banwell, B, Blaser S, Tsui L-C, Teebi AS: The locus responsible for horizontal gaze palsy/progressive scoliosis and brainstem hypoplasia is refined to a 9cM region on chromosome 11q23. Clinical Genetics 2004: 65(2): pp 137. SRI 174. Al-Mulla N, Belgaumi AF, Teebi AS: Cancer in Sotos Syndrome: report of a patient with acute myelocytic leukaemia and review of literature. Journal of Paediatric Hematology and Oncology 2004: 26(3): pp 204-208. CPA 175. Teebi AS, Dupuis L, Wherrett D, Khoury A, Zucker KJ: Alopecia, microcephaly, larngomalacia, cutis marmorata, short stature and XY gonadal dysgenesis: El-Shanti syndrome. European Journal of Pediatrics 2004: 163(3): pp 170. PA 176. Teebi AS: Naming of a syndrome: The story of Adam Wright syndrome. American Journal of Medical Genetics 2004: 125(A): pp 329. PA 177. Kennedy SJ, Teebi AS: Newly Recognized Autosomal Recessive Acrofacial Dysostosis Syndrome Resembling Nager Syndrome. American Journal of Medical Genetics 2004: 129A: pp 73-76. SRI 178. Faiyaz-Ul-Haque M, Zaidi SHE, Al-Ali M, Al-Mureikhi M, Kennedy S, Al Thani G, Tsui L-C, Teebi AS: A novel missense mutation in the galactosyltransferase I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers-Danlos syndrome resembling the progeroid type. American Journal of Medical Genetics 2004: 128A(1): pp 39-45. SRI 179. Walker LC, Teebi AS, Marini JC, Paepe AD, Malfait F, Atsawasuwan P, Yamauchi M, Yeowell HN: Decreased expression of lysyl hydroxylase 2 (LH2) in skin fibroblasts from three Ehlers-Danlos patients does not result from mutations in either the coding or proximal promoter region of the LH2 gene. Mol Genet Metab 2004: 83: pp 312-21. C
  19. 19. 180. * - Lemire BD, Kennedy SJ, Teebi AS: Congenital mydriasis, patent ductus arteriosus, and congenital cystic lung disease: New syndromic spectrum? American Journal of Medical Genetics 2004: 131A: pp 318-319. SRI 181Zaidi SHE, Peltekova V, Meyer S, Lindinger A, Paterson AD, Tsui L-C, Faiyaz-Ul-haque, Teebi AS: A family exhibiting arterial tortuosity syndrome displays homozygosity of markers associated with arterial tortuosity locus at chromosome 20q12. Clinical Genetics 2005: 67(2): pp 183-188. CPA 182Teebi AS, Teebi SA: Genetic diversity among the Arabs. Community Genetics 2005: 8: pp 21-26. PA 183. *Ben Omran T, Teebi AS: Structural CNS anomalies in Kabuki syndrome. American Journal of Medical Genetics 2005: 137A pp 100-103 PA 184.Faqeih E, Sakati N, Teebi AS: Meier-Gorlin Syndrome: Previously unrecognized findings. American Journal of Medical Genetics 2005: 137: pp339-341. SRI 185. Minrong A, Heeger S, Bartels, CF, Schelling DK, and the Osteoporosis-Pseudoglioma Collaborative Group: Clinical and Molecular Findings in Osteoporosis-Pseudoglioma Syndrome. Am. J. Hum. Genet 2005: 77:741-753.C 186.Al-Mayouf S, Bahabri S, Sakati N, Teebi AS: Infantile systemic hyalinosis. A fatal disorder commonly diagnosed among the Arabs. Clinical Experimental Rheumatology 2005: 23: pp717-720 CPA Submitted 1. Chan JM, Teebi AS, Siu VM: The syndrome of multiple circumferential skin creases, MCA, variable MR in two Mennonite brothers. Clinical Dysmorphology. CPA Non Peer Reviewed - Journal Publications Published 1. Teebi AS: Blending bytes and book: Medical Genetics: A self-instruction guide and workbook based on Mendelian inheritance in man by Victor McKusick, 1993 (Book review). Trends in Endocrinology and Metabolism 1994: 5(8): pp 354. PA 2. Fathalla D, Dellagi Q, Qumsiyeh M, Teebi AS: Recent advances in Molecular genetics of the Maghreb and The Middle East population: Conference report: First MEGA Conference, Tunisia, 1997. American Journal of Medical Genetics 1997: 78: pp 90-91. SRI 3. Teebi AS: (Book Review) A clinical guide to inherited metabolic diseases by JTR Clarke, 1996. American Journal of Medical Genetics 1998: 78: pp 94. PA
  20. 20. 4. Teebi AS, Shawky R: Population and molecular genetic update: The second Middle East Genetics Association (MEGA) Conference. American Journal of Medical Genetics 2000: 92: pp 293-294. PA 5. Teebi AS: (Book Review) Health and Ethnicity. Edited by H. Macbeth & P. Shetti Taylor & Francis, London & New York, 2001. Am J. Medical Genetics 2003: 127A: pp 217. PA 6. *Chun K, Teebi AS, Teshima I: Response to correspondence from Gripp et al. - "clinical and molecular diagnosis should be consistent". American Journal of Medical Genetics 2003: 122A(1): pp 91. CPA 7. Teebi AS: Reply to Ruiter et al: A possible example of Acrofacial Dysostosis Type Kennedy-Teebi. American Journal of Medical Genetics. 2005 PA Books/Chapters in Books/Proceedings Published 1. Teebi AS: Dissertation - Therapy of inherited metabolic phenotypes by dietary supplementation - July 1983 London, England 1983. PA 2. Al-Awadi SA, Teebi AS, Farag TI, Naguib KK: Inherited metabolic disease in Kuwait: The need for a nation wide neonatal screening. In: Advances in Neonatal Screening (Therrell, ed). Elsevier Science Publisher, B.V. Amsterdam479-480%1988-890 1987: pp 479-480. CPA 3. Palcovic M, Yadav G, Gumma, Bahman, Abu Farsakh, Teebi AS: Laboratory Manual for Screening and Detection of Inherited Metabolic Diseases Kuwait Group of Clinical Biochemists' Publications (Palcovic, Yadav, Gumma, Bahman, Abu Farsakh, Teebi, eds). Kuwait group of clinical biochemists' publications, Kuwait 1988: pp 66. CPA 4. Teebi AS, Al-Awadi SA, Al-Awqati MA, Farag TI, Naguib KK: Neonatal screening for phenylketonuria and congenital hypothyroidism in Kuwait: A preliminary report. In: Neonatal Screening. Proceedings of the 6th National Screening Symposium (Skeels, Buist, Tureck, eds). Portland, Oregon 1988: pp 150-151. PA 5. Teebi AS: Microcephaly, autosomal recessive with normal intelligence. In: Birth Defects Encyclopedia Alan R Liss, New York, NY 1990. PA 6. Teebi AS, Al-Awadi SA: Ulnar-Fibular absence - Severe limb defect. In: Birth Defects Encyclopedia Alan R Liss, New York, NY 1990. PA 7. El-Badramany MH, Farag TI, Al-Awadi SA, Teebi AS: Psychosocial and medical aspects of genetic counselling among the Arabs: The example of Kuwait. In: Genetic Disorders Among Arab Populations - Oxford Monograph on Medical Genetics no.30. (Teebi AS, Farag
  21. 21. TI, eds). Oxford University Press, New York, NY 1997: pp 474-486. CPA 8. Farag TI, Teebi AS: Genetic Disorders among the Bedouin. In: Genetic Disorders Among Arab Populations - Oxford Monograph on Medical Genetics no.30. (Teebi AS, Farag TI, eds). Oxford University Press, New York, NY 1997: pp 375-410. CPA 9. Qumsiyeh M, Dasouki M, Teebi AS: Genetic Disorders among Palestinians and Jordanians. In: Genetic Disorders Among Arab Populations - Oxford Monograph on Medical Genetics no.30. (Teebi AS, Farag TI, eds). Oxford University Press, New York, NY 1997: pp 227-259. SRI 10. Teebi AS: Genetic Disorders among Arab populations: Introduction. In: Genetic Disorders Among Arab Populations - Oxford Monograph on Medical Genetics no.30. (Teebi AS, Farag TI, eds). Oxford University Press, New York, NY 1997: pp 1-26. PA 11. Teebi AS: New disorders first recognized among Arabs. In: Genetic Disorders Among Arab Populations - Oxford Monograph on Medical Genetics no.30. (Teebi AS, Farag TI, eds). Oxford University Press, New York, NY 1997: pp 159-190. PA 12. Teebi As: Overview of genetic and malformation syndromes in Arab populations. In: Proceedings of the Greenwood Genetic Center (Blackburn W, Phelan MC, eds). 1997. PA 13. Teebi AS, Eliott AM, Fraser FC: Severe microcephaly, wide eyebrows, large ears, developmental retardation and other anomalies in two unrelated children: New syndrome? In: Proceedings of the Greenwood Genetic Center (Blackburn W, Phelan MC, eds). 1997. PA 14. Teebi AS, Farag TI: Genetic Disorders Among Arab Populations - Oxford Monograph on Medical Genetics no.30. (Teebi AS, Farag TI, eds). Oxford University Press, New York, NY 1997: pp 499. PA 15. Teebi AS, Tewfik TL, Der Kaloustian VM: Syndromes and conditions associated with anomalies of the neck. In: Congenital Anomalies of Ear, Nose and Throat (Tewfik TL, Der Kaloustian VM, eds). Oxford University Press, NY 1997: pp 361-376. PA 16. Teebi AS, Tewfik TL, Der Kaloustian VM: Syndromes and conditions associated with congenital anomalies of the nasopharynx and sinuses. In: Congenital Anomalies of Ear, Nose and Throat (Tewfik TL, Der Kaloustian VM, eds). Oxford University Press, NY 1997: pp 201-228. PA 17. Tewfik TL, Teebi AS, Der Kaloustian VM: Selected syndromes and conditions. In: Congenital Anomalies of Ear, Nose and Throat (Tewfik TL, Der Kaloustian VM, eds). Oxford University Press, NY 1997: pp 441-546. CPA 18. Tewfik TL, Teebi AS, Der Kaloustian VM: Syndromes and conditions associated with congenital anomalies of the ear. In: Congenital Anomalies of Ear, Nose and Throat (Tewfik TL, Der Kaloustian VM, eds). Oxford University Press, NY 1997: pp 125-144. CPA 19. Tewfik TL, Teebi AS, Der Kaloustian VM: Syndromes and conditions associated with congenital anomalies of the larynx and trachea. In: Congenital Anomalies of Ear, Nose and
  22. 22. Throat (Tewfik TL, Der Kaloustian VM, eds). Oxford University Press, NY 1997: pp 393-400. CPA 20. Tewfik TL, Teebi AS, Der Kaloustian VM: Syndromes and conditions associated with congenital anomalies of the mouth, palate and pharynx. In: Congenital Anomalies of Ear, Nose and Throat (Tewfik TL, Der Kaloustian VM, eds). Oxford University Press, NY 1997: pp 263-286. CPA 21. Tewfik TL, Teebi AS, Der Kaloustian VM: Syndromes and conditions associated with Genetic Deafness. In: Congenital Anomalies of Ear, Nose and Throat (Tewfik TL, Der Kaloustian VM, eds). Oxford University Press, NY 1997: pp 145-182. CPA 22. Tewfik TL, Teebi AS, Der Kaloustian VM: Syndromes and conditions associated with tracheoesophageal fistula or abnormal esophagus. In: Congenital Anomalies of Ear, Nose and Throat (Tewfik TL, Der Kaloustian VM, eds). Oxford University Press, NY 1997: pp 433-441. CPA 23. * - Graham G, Teebi AS: An approach to the dysmorphic infant or child. In: Textbook of Clinical Pediatrics (Harfi, Nazer, Zouki, eds). Lippincott, Williams & Wilkins, Philadelphia, PA 2001: pp 3-19. SRI 24. Elliott A, Teebi AS: Genetic Counselling. In: Textbook of Clinical Pediatrics (Harfi, Nazer, Zouki, eds). Lippincott, Williams & Wilkins, Philadelphia, PA 2001: pp 33-38. SRI 25. Qumsiyeh MB, Teebi AS: Cytogenetics. In: Textbook of Clinical Pediatrics (Harfi, Nazer, Zouki, eds). Lippincott, Williams & Wilkins, Philadelphia, PA 2001: pp 20-32. SRI 26. Teebi AS: Genetic Disorders - Section Leader. Textbook of Clinical Pediatrics (Harfi, Nazer and Elzouki, eds). Lippincott, Williams and Wilkins, Philadelphia, PA 2001: pp 3-38. PA 27. Teebi AS, Kennedy S, Chun K, Ray P: Severe and mild phenotypes in Pfeiffer syndrome: Report of two novel mutations in FGFR2 gene. In: Proceedings of the Greenwood Genetic Center San Diego, Ca 2001: pp pp 164. PA 28. * - Bedford HM, Teebi AS: Adams-Oliver Syndrome. In: The Nord Guidebook for Rare Disorders (Gruson, E, eds). Lippincott, Williams & Wilkins, Philadelphia 2003: pp 148. SRI 29. Nezarati MM, Teebi AS: Ear-Patella short stature syndrome. In: The Nord Guidebook to Rare Disorders. (Gruson, Edward, eds). Lippincott, Williams & Wilkins, Philadelphia 2003: pp 189. CPA 30. Teebi AS, Kennedy SJ: Autosomal recessive traits and diseases. In: Nature Encylopedia of Life Sciences. 2005 PA 31. Teebi AS, Kennedy SJ, Chitayat D, Teshima I, Unger S, Babul-Hirji R, Shuman C, Weksberg R: Clinical Genetics. In: Hospital for Sick Children, Atlas of Paediatrics (Laxer R, Lee Ford Jones E, Friedman J, Gerstle T, eds). 2005 Current Medicine Inc, New York pp
  23. 23. 1-33. PA Abstracts 1. Al-Awadi SA, Farag TI, Naguib KK, Teebi AS: Six hemizygous male sibs with X-linked hydrocephalus. Clinical Genetics 1983: 23(3): pp 224. SRI 2. Al-Awadi SA, Naguib KK, Farag TI, Teebi AS: Three sibs with Aarskog-Scott syndrome. Clinical Genetics 1983: 23(3): pp 223. SRI 3. Al-Awadi SA, Teebi AS, Farag TI, Naguib KK: PKU & hypoparathyroidism among mentally retarded in Kuwait. Abstract Book of the 7th World Congress of the International Association for the Scientific Study of Mental Deficiency, New Delhi. 1985: pp 3. CPA 4. Naguib KK, Farag TI, Al-Awadi SA, Teebi AS et al: Major congenital malformations among live births in Kuwait. American Journal of Human Genetics 1986: 39(3): pp S-A73. C 5. Farag TI, Al-Awadi SA, Teebi AS et al: Rare chromosomal syndromes in Kuwait: A seven-year experience. American Journal of Human Genetics 1986: 39(3): pp S-A113. C 6. Teebi AS, Krishna Murthy DS, Sundareshan TS: Mosaic 45X, 46XY and unusual aberrations of Y chromosome in a male with short stature, hypospadias and infertility. American Journal of Human Genetics 1987: 41(3): pp A142(418). PA 7. Al-Awadi SA, Farag TI, Teebi AS, Naguib KK, El-Khalifa MY et al: Cytogenetic profile of Down syndrome in Kuwait: A decade of experience. Proceedings of the international conference of Human Genetics and Anthropology, University of Cairo, Cairo, Egypt. 1989. C 8. * - El-Khalifa MY, Farag TI, Naguib KK, Teebi AS et al: Early diagnosis of hermaphroditism in a mixed Arab population. American Journal of Human Genetics 1989: 45: pp A44(0167). C 9. Teebi AS, Farag TI: New monogenic disorders in a mixed Arab population. American Journal of Human Genetics 1989: pp A66(0252). PA 10. Farag TI, Teebi AS: Observations on cystic fibrosis in Kuwait. American Journal of Human Genetics 1989: pp A238(0936). SRI 11. Teebi AS, Al-Saleh QA: Mandibuloacral dysplasia: Varied presentation. Proceedings of the 8th International Congress of Human Genetics, 1991: pp 167 (A878). PA 12. * - Kogekar N, Teebi AS, Vockley J: Delineation of the sandrow syndrome. American Journal of Human Genetics 1992: 51(4): pp A305(1201). CPA 13. Al-Awadi SA, Othman SA, Mohamed FM, Abul Hasan SJ, Redha AA, Farag TI, Naguib KK, Teebi AS et al: Kuwait Cytogenetic Registry. 11th International Chromosome
  24. 24. Conference, Edinburgh. 1992: pp A2, 71. C 14. Teebi AS, Gibson L, McGrath J, Meyn MS, Breg TL, Yang-Feng T: Molecular and cytogenetic characterization of 9p- abnormalities. Report of 2 patients. American Journal of Human Genetics 1992: 51(4): pp A89(342). PA 15. * - Chu TW, Teebi AS, Gibson L, Breg TL, Yang-Feng T: "C" phenotype with complex chromosome rearrangement resulting in partial trisomy 13 and partial tetrasomy 13 delineated by FISH analysis. American Journal of Human Genetics 1993: 53(3)Supp: pp A534. CPA 16. Rupps R, Teebi AS: A syndrome of generalized obesity and minor facial and limb anomalies in 5 generations. American Journal of Human Genetics 1994: 55(3)Supp: pp 1822 A311. SRI 17. * - Al-Fifi S, Shevell M, Al-Ata J, Teebi AS: A three-generation family with the Silver- Russell syndrome. American Journal of Human Genetics 1994: 55(3)Supp: pp 424 A77. SRI 18. Ross M, Pinsky L, Teebi AS, Zaor S, Eydoux P: De novo partial duplication 7(q11.2- >q21.2) in a dysmorphic and developmentally retarded boy. American Journal of Human Genetics 1994: 55(3)Supp: pp 1884 A322. C 19. * - Al-Ata J, Paquet M, Teebi AS: Double outlet right ventricle in Robinow syndrome. American Journal of Human Genetics 1994: 55(3)Supp: pp 1790 A306. SRI 20. Elliot AM, Teebi AS: MCA/MR syndrome with features of Michelin Tire baby syndrome. American Journal of Human Genetics 1994: 55(3)Supp: pp 1801 A308. CPA 21. Teebi AS, Watters G, Eydoux P, Oudjahne K, Sajoo A: Spastic paraplegia, dysarthia, and optic atrophy in phenotypic female siblings discordant for XY gonadal dysgenesis. American Journal of Human Genetics 1994: 55(3)Supp: pp 527 A94. PA 22. * Hoodfar E, Teebi AS: Genetic referrals of Middle Eastern origin in a western city: Inbreeding and disease profile. American Journal of Human Genetics 1995: 57(4): pp 1841, A317. SRI 23. * - Sasi R, Rosenfeld B, Eydoux P, Teebi AS: Heterogeneity of trichothiodystrophy- neurocutaneous syndrome. American Journal of Human Genetics 1995: 57(4): pp 1783, A307. SRI 24. Teebi AS, Elliott AM: Microcephaly, microtia, cleft palate, severe mandibular hypoplasia, limb anomalies and short stature: Possible new autosomal recessive syndrome resembling the Ear-Patella-Short Stature Syndrome. American Journal of Human Genetics 1995: 57(4): pp 576, A104. PA 25. * - Al-Ghamdi MA, Polomeno R, Chitayat D, Azouz M, Teebi AS: Pena-Shokeir phenotype with normal intelligence. American Journal of Human Genetics 1995: 57(4): pp 1767, A305. SRI
  25. 25. 26. * - Kaurah P, Teebi AS: Total Anonychia congenita and microcephaly with normal intelligence in 2 siblings of consanguineous parents. A new autosomal recessive syndrome? American Journal of Human Genetics 1995: 57(4)Supp: pp A94. SRI 27. Teebi AS: Genetic disorders among the Arabs and Arabian Influence in European Population. Conference on Inherited Disorders and their genes, Barcelona, Spain. European Populations 1995. PA 28. Robb L, MacPhee N, Elliott AM, Teebi AS: A clinogenetic study of familial primary microcephaly. American Journal of Human Genetics 1996: 59(4)Supp: pp A102. SRI 29. * - Graham GE, Brown GK, Robinson BH, Treacy EP, Zvi RT, Teebi AS: Features of Ruvalcaba-Mhyre-Smith syndrome with oligodactyly of the toes and functional PDH deficiency: Clinical heterogeneity or new syndrome. American Journal of Human Genetics 1996: 59(4)Supp: pp A350. SRI 30. Eydoux P, Sanderson D, Treacy E, Scriver C, Teebi AS: HHH-like syndrome and dysmorphic features associated with 22q deletion: A new contiguous gene syndrome. American Journal of Human Genetics 1996: 59(4) Supp: pp A117. SRI 31. Elliott AM, Teebi AS, Fraser FC: Severe microcephaly, thick eyebrows, large ears, developmental retardation and other anomalies in two unrelated children: New syndrome. American Journal of Human Genetics 1996: 59(4)Supp: pp A92. CPA 32. Teebi AS: An overview on genetic and malformation syndromes among the Arabs. David Smith Workshop on malformations and morphogenesis, Lake Arrowhead, CA. 1996: pp 110. PA 33. Teebi AS, Graham GE, Brown GK, Robinson BH, Treacy EP, Zori RT: Features of Ruvalcaba-Myhre-Smith Syndrome with oligodactyly of the Toes and Functional PDH Deficiency: Clinical Heterogeneity or New Syndrome? David W. Smith Workshop on Malformations and Morphogenesis, Lake Arrowhead, CA. 1996: pp 96. PA 34. Teebi AS, Elliott AM, Fraser FC: Severe Microcephaly, Wide Eyebrows, Large Ears, Developmental Retardation and Other Anomalies in Two Unrelated Children: New Syndrome? David W. Smith Workshop on Malformations and Morphogenesis, Lake Arrowhead, CA. 1996: pp 173. PA 35. Elliott AM, Graham GE, Bernstein ML, Teebi AS: Dyskeratosis Congenita: An autosomal recessive entity. American Journal of Human Genetics 1997: 61(4)Supp: pp A97. SRI 36. Teebi AS: Genetic and malformation syndromes in Arab populations: An overview and update. Les Arch de L'Institut Pasteur de Tunis, LXXIV, 1997: 3/4: pp 23. PA 37. Eydoux P, Hewson S, Scarpelli H, Halal F, Teebi AS: Juberg-Marsidi Syndrome associated with an inherited paracentric inversion of chromosome X. American Journal of Human Genetics 1997: 61(4)Supp: pp A124. SRI
  26. 26. 38. Azouz EM, Teebi AS: New autosomal dominant rhizomesomelic short stature syndrome. American Journal of Human Genetics 1997: 61(4)Supp: pp A91. SRI 39. Teebi AS, Rajchgot H: New autosomal dominant syndrome of hypertelorism and nasolacrimal duct dysgenesis. American Journal of Human Genetics 1997: 61(4)Supp: pp A115. PA 40. Teebi AS, Elliott AM, Fraser FC: Severe microcephaly, wide eyebrows, large ears, developmental retardation and other anomalies in two unrelated children new syndrome. Editors: Blackburn W, Phelan MC, Proceedings of the Greenwood Genet Center 1997: 16: pp 251. PA 41. Elliott AM, Teebi AS: An autosomal dominant syndrome reminiscent of Noonan syndrome and Coffin-Siris syndrome. American Journal of Human Genetics 1998: 63(4)Supp: pp A103. SRI 42. * - Al-Ata J, Noreau DR, Gowans GC, Teebi AS: Congenital heart disease in Sotos overgrowth syndrome. American Journal of Human Genetics 1998: 63(4)Supp: pp A95. SRI 43. * - Al-Mohri H, Al Fifi S, Teebi AS: Setleis "Forceps Marks" syndrome: A recognizable Gestalt. American Journal of Human Genetics 1998: 63(4)Supp: pp A96. SRI 44. Teebi AS, Cartier L, Azouz EM: The expanded spectrum of pentalogy of Cantrell. American Journal of Human Genetics 1998: 63(4)Supp: pp A122. SRI 45. Teebi AS: Establishing genetic service in a Gulf country. 12th International Child Health Conference, Muscat, Oman. 1999. PA 46. Teebi AS: Genetic diversity among the Arabs. Lesson from PAH & CF genes. 12th International Child Health Conference, Muscat, Oman. 1999. PA 47. Kennedy SJ, Chan A, Al-Sannaa N, Teshima I, Teebi AS: Fryns syndrome or Pallister Killian syndrome (Tetrasomy 12p)? The importance of delineation. American Journal of Human Genetics 1999: 65(4)Supp: pp A154. SRI
  27. 27. 48. * - Chun KM, Teebi AS, Kennedy SJ, Forrest CR, Ray PN: Graduated strategy for the molecular diagnosis of craniosynostosis syndromes. American Journal of Human Genetics 1999: 65(4)Supp: pp A289. SRI 49. Elliott AM, Azouz E M, Teebi AS: Progressive Erosive Arthropathy, characteristic non- coarse facies, malar erythema, facial telangiectasia, and multiple nevi: A new syndrome? American Journal of Human Genetics 1999: 65(4)Supp: pp A148. SRI 50. * - Al-Sannaa N, Teebi AS: Severe micrognathia, large ears, atrioventricular, septal defect, symmetrical cutaneous syndactyly of hands and multiple cafe-au-lait spots: A new syndrome? American Journal of Human Genetics 1999: 65(4)Supp: pp A140. SRI 51. * - Siriwardena K, Babul R, Chitayat D, Cytrynbaum CS, Dupuis L, Emanuel BS, Kennedy SJ, Kurahashi H, Nie G, Teebi AS, Weksberg R, Winsor E, Teshima I: Spectral karyotyping for marker chromosomes. American Journal of Human Genetics 1999: 65(4)Supp: pp A357. C 52. Teebi AS, Al-Sannaa N, Adatia I: Transverse limb defects associated with vascular abnormalities: Atypical presentation of Adams-Oliver syndrome? American Journal of Human Genetics 1999: 65(4)Supp: pp A346. PA 53. * - Gowans GC, Goncalves S, Duncan AMV, Eydoux P, Teebi AS: Two cases of partial Trisomy 8 and 14 (8q24.1-->qter and 14pter-->q22) with semilobar holoprosencephaly and comparisons to Seckel syndrome. American Journal of Human Genetics 1999: 65(4)Supp: pp A150. SRI 54. Teebi AS: Dysmorphology: The Art and Science. The 2nd MEGA Conference joint with Ain Shams University, Cairo, Egypt. 1999. PA 55. Teebi AS: The diversity of the Arabs: Lessons from genetic studies. The 2nd MEGA Conference joint with Ain Shams University, Cairo, Egypt. 1999. PA 56. Quercia NL, Teebi AS: Craniosynostosis, ectopia lentis and congenital heart defect: further delineation of an autosomal dominant syndrome with reduced penetrance. Genetics in Medicine 2000: 2: pp 85. SRI 57. * - Lo B, Blazer S, Banwell B, Quercia N, Teebi A: Ophthalmoplegia: severe scoliosis and brain stem hypoplasia: A recognized autosomal recessive syndrome. American Journal of Human Genetics 2000: 67(4)Supp: pp A543. SRI 58. Kennedy SJ, Wei C, Steele L, Teebi AS: Prenatal diagnosis of fragile X syndrome: Identification of a male fetus mosaic for premutation on chorionic villus sampling management and follow up. Genetics in Medicine 2000: 2: pp 101. SRI 59. Teebi AS, Kennedy S, Chun K, Ray P: Severe and mild phenotypes in Pfeiffer syndrome: Report of two novel mutations in FGFR2 gene. San Diego, CA. XXI David Smith Workshop 2000. PA
  28. 28. 60. Teebi AS, Teebi SA, Porter C, Cuticchia AJ: Arab Genetic Database (AGDDB) Mutation Database Initiative. American Society of Human Genetics Annual Meeting, Philadelphia, Pennsylvania. 2000. CPA 61. Teebi AS: Genetic Counseling among the Arabs. The 2nd Arabian Gulf Medical Assocation's Conference, Abu Dhabi, UAE. 2000. PA 62. Teebi AS: Genetic disorders among Arabian Gulf populations. The 2nd Arabian Gulf Medical Association's Conference, Abu Dhabi, UAE. 2000. PA 63. Teebi AS, Kennedy S, Chun K, Ray P: Severe and mild phenotypes in Pfeiffer syndrome: Report of two novel mutations in FGFR2 gene. Proceedings of the Greenwood Genetic Center, San Diego, CA. 2001: 20: pp 164. PA 64. Teebi AS: Genetic disorders among Arab children. Pediatrics at a glance symposium, King Faisal Specialist Hospital & Research Center, Jeddah, SA. 2001. PA 65. Teebi AS: Genetic Epidemiology of the Mediterranean population. Euro-Med Genetic Workshop, Tunis, Tunisia. 2001. PA 66. Teebi AS: The dysmorphology approach. Pediatrics at a glance symposium, King Faisal Specialist Hospital & Research Center, Jeddah, SA. 2001. PA 67. Teebi AS: Genetic screening and testing: The Canadian experience. Premarital counseling symposium, Jeddah, SA. 2001. PA 68. * - Azimi C, Kennedy SJ, Forrest C, Teebi AS: Clinical and Genetic Aspects of Trigonocephaly: A Study of 22 Cases. American Society of Human Genetics 51st Annual Meeting, San Diego, Ca. The American Journal of Human Genetics 2001: 69: pp 286. SRI 69. UL Haque MF, Ahmad W, Zaidi SHE, Haque A, Wahab A, Azimi AC, Teebi AS, Ahmad M, Cohn DH, Siddique T, Tsui LC: Mutations in the Cartilage Derived Morphogenetic Protein-1, in kindred affected with Grebe Type severe short limb dwarfism and DuPan Syndrome. American Society of Human Genetics 51st Annual Meeting, San Diego, Ca. The American Journal of Human Genetics 2001: 69: pp 630. C 70. Kennedy SJ, Teebi AS: New autosomal recessive syndrome resembling Nager syndrome. American Society of Human Genetics 51st Annual Meeting, San Diego, Ca. The American Journal of Human Genetics 2001: 69: pp 290. PA 71. Dupuis L, Teebi AS, Nezarati MM: Rhizomelic Limb Shortness in NF1: A Previously Unrecognized Skeletal Manifestation? American Society of Human Genetics 51st Annual Meeting, San Diego, Ca. The American Journal of Human Genetics 2001: 69: pp 277. CPA 72. Teebi AS, Teebi SA, Porter CJ, Cuticchia AJ: The Arab Genetic Disease Database: A National Database of Genetic Disorders. American Journal of Human Genetics, San Diego, CA. American Society of Human Genetics, 51st Annual Meeting 2001: 69: pp 391. SRI
  29. 29. 73. Teebi AS: Genetic databases. Conference in Child Health and the 9th Conference of the Union of Arab Pediatric Societies, Jeddah, SA. 2001. PA 74. Teebi AS: The dysmorphology approach. Conference in Child Health and the 9th Conference of the Union of Arab Pediatric Societies, Jeddah, SA. 2001. PA 75. Teebi AS: Cardinal signs and emerging genotype-phenotype association: Teebi Hypertelorism. Annual Clinical Genetics Meeting, New Orleans, LI. American College of Medical Genetics 2002. PA 76. Teebi AS: Cardinal signs and emerging genotype-phenotype association: The Bartsocas Papas Syndrome. Annual Clinical Genetics Meeting, New Orleans, LI. American College of Medical Genetics 2002. PA 77. *Al-Sanna NA, Teebi AS: Bilateral congenital ptosis and variable toe anomalies: a new autosomal recessive syndrome? ESHG meeting, Strasbourg, France. 2002. CPA 78. Ul Haque MF, Abdul Wahab A, Janahi IH, Zaidi, SHE, Teebi AS, Tsui LC: A novel Ehlers-Danlos-like syndrome with vascular abnormalities and tortuous systemic arteries: Linkage analysis. The American Society of Human Genetics, 52nd Annual meeting, October 15-19, 2002., Baltimore, Maryland. American Journal of Human Genetics 2002: 71(4): pp 263. SRI 79. Abdul Waham A, Janahi IA, Ul Haque F, Eltohami A, Zeid A, Teebi AS: A New Type of Ehlers-Danlos Syndrome Associated with tortuous Systemic Arteries in a Qatari extended family. Doha, Qatar. Qatar Medical Journal 2002: 11(2): pp 76. SRI 80. *Penney L, Kennedy SJ, Teebi AS: Lambdoid craniosynostosis and hypospadias - a new syndrome? Abstract # 88. Annual Clinical Genetics Meeting in cooperation with the 34th Annual March of Dimes Clinical Genetics Conference, San Diego, CA. 2003: pp 67. SRI 81. Yeowell HN, Walker, LC, Teebi AS: Severely reduced levels of the mRNAs for lysyl hydroxylase 2 (LH2) in 3 patients with Ehlers-Danlos-like symptoms do not result from mutations in the coding region for LH2. Society of Investigative Dermatology, Miami, Fl. J. Invest. Dermatol 2003: 121: pp 602. C 82. Teebi AS: Genetic disorders among Arabs. The 1st GCC Genetic Conference, Bahrain. 2003. PA 83. Mueller RE, Nie G, Nezarati MM, Dupuis L, Teebi AS, Kennedy SJ, Chitayat D, Stephens D, Shago M, Teshima I: Selection of patients with idiopathic mental retardation for subtelomeric FISH analysis: Experience at Hospital for Sick Children, Toronto. 2003 Annual Scientific Meeting, Edmonton, AB. Canadian College of Medical Geneticists 2003: 03: pp 15. C
  30. 30. 84. Ul Haque MF, Teebi AS, Al-Ali M, Al-Mureikhi MS, Kennedy SJ, Al-Thani G, Zaidi SHE, Tsui L-C: A Novel Homozygous Recessive Mutation in the Galactosyltransferase-I (B4GALT7) Gene in Individual Resembling the Progeroid Type of Ehlers-Danlos syndrome. The American Society of Human Genetics, Los Angeles, CA. The American Journal of Human Genetics 2003: 73(5): pp 563. SRI 85. Teebi AS: Hypertelorism syndrome: Proposed nosology. Society of Craniofacial Genetics, Los Angeles, CA. 2003. PA 86. Mueller RE, Nie G, Nezarati MM, Dupuis L, Teebi AS, Kennedy SJ, Chitayat D, Stephens D, Shago M, Teshima I: Selection of patients with idiopathic mental retardation for subtelomeric FISH analysis: Experience at Hospital for Sick Children, Toronto. The American Society of Human Genetics, Los Angeles, CA. The American Journal of Human Genetics 2003: 73(5): pp 305. C 87. Teebi AS: Genetic diversity among the Arabs. International Genetics Congress, Dubai, UAE. 2003. PA 88. Teebi AS: Neurodevelopment and dysmorphology: Clues for diagnosis. International Genetics Congress, Dubai, UAE. 2003. PA 89. Teebi AS: Patterns of genetic disorders among the Arabs. Workshop on Genetic disorders in the Arab world, Dubai, UAE. 2003. PA 90. Teebi AS: An approach to the child with birth defects. 4th International Symposium on recent advances in Pediatrics, Jeddah, SA. 2004. PA 91. Teebi AS: Developmental delay and dysmorphology: Clues for diagnosis. 4th International Symposium on recent advances in Pediatrics, Jeddah, SA. 2004. PA 92. Teebi AS: Molecular genetic diagnostics for Pediatricians: An update. 4th International Symposium on recent advances in Pediatrics, Jeddah, SA. 2004. PA 93. Al-Sanna'a NA, Teebi AS: Trigonocephaly, variable limb anomalies, cutis laxa: A new autosomal recessive syndrome? European Human Genetics Conference 2004, Munich, Germany. European Journal of Human Genetics 2004: 12: pp P0012. CPA 94. Zaidi SHE, Peltekova V, Meyer S, Lindinger A, Paterson AD, Tsui L-C, Teebi AS, Ul Haque MF: A family exhibiting arterial tortuosity syndrome displays homozygosity of microsatellite markers associated with the arterial tortuosity locus. American Society of Human Genetics 54th Annual Meeting, Toronto, ON. 2004: pp 133, A633. SRI 95. *Faqeih E, Sakati N, Teebi AS: Meier-Gorlin Syndrome (Ear-Patella-Short Stature Syndrome): Growth Hormone Deficiency and Previously Unrecognized Findings. American Society of Human Genetics 54th Annual Meeting, Toronto, ON. 2004: pp 139, A669. SRI
  31. 31. 96. Hamamy H, Ajlouni K, Teebi AS: Midface Prominence, Dental/Enamel Hypoplasia, Prominent/Simple Ears, Osteopenia with Repeated Fractures and Borderline Intelligence in Two Brothers: New Syndrome or An Association of Two Distinct Syndromes? American Society of Human Genetics 54th Annual Meeting, Toronto, ON. 2004: pp 139, A669. CPA 97. Al-Hassnan ZN, Teebi AS: New Syndrome of Craniofacial Anomalies, Radiohumeral Synostosis and Rhizomelic Shortness. American Society of Human Genetics 54th Annual Meeting, Toronto, ON. 2004: pp A770. CPA 98. Klatt R, Velsher L, Dyack S, Ray P, Steele L, Barozzino T, Sgro M, Teebi AS, Chitayat D: Prader-Willi syndrome with multi-suture craniosynostosis: Report of two cases. American Society of Human Genetics 54th Annual Meeting, Toronto, ON. 2004: pp 141, A678. C 99. *Ben-Omran T, Teebi AS: Structural central nervous system (CNS) anomalies in Kabuki make-up syndrome. American Society of Human Genetics 54th Annual Meeting, Toronto, ON. 2004: pp A830. PA 100. Teebi AS, Haroun I, Ahmed I, Al-Mureikhi M, Salem MSZ, Al-Thani G: Teebi-Shaltout Syndrome: A Report of Further Arab Patients. American Society of Human Genetics 54th Annual Meeting, Toronto, ON. 2004: pp 145, A703. PA 101. *Al-Sanna'a N, Al-Khunaizi M. Teebi AS: Trigonocephaly, Polysyndactyly, Brachdactyly, Cutis Laxa and Developmental Delay. American Society of Human Genetics 54th Annual Meeting, Toronto, ON. 2004: pp 137, A 657. SRI 102. Fishman LL, Maegawa G, Babul-Hirji R, Chitayat D, Teebi AS: Two cases of chromosome 8p23 deletion with different clinical presentation. American Society of Human Genetics 54th Annual Meeting, Toronto, ON. 2004: pp A682. C 103. Kim LE, Klatt R, Teebi AS: Cleft lip and palate and syndactyly in a father and son: new syndromic association? European Human Genetics Conference, Prague, Czech Republic. European Journal of Human Genetics 2005: 13(1): pp 86(#P0032). SRI 104. Al-Sanna'a NA, Al-Dhafiri SA, Teebi AS: Poikiloderma, alopecia, bilateral optic nerve atrophy, cerebral calcification, and bone marrow suppression: severe Rothmund Thomson Syndrome? European Human Genetics conference, Prague, Czech Republic. European Journal of Human Genetics 2005: 13(1): pp 85(#P0025). CPA 105.T. Ben-Omran, Teebi AS: Structural central nervous system (CNS) anomalies in Kabuki make-up syndrome. European Human Genetics Conference, Prague, Czech Republic. European Journal of Human Genetics 2005: 13(1): pp 81(#P0005). SRI 106.Ul Haque M, Zaidi SHE, Al-Mureikhi M, Al-Thani G, Tsui L-C: Mutation Hot-spot in CHX10 Gene Associated with Non-syn dromic Microphthalmia in Qatari Families. Annual Meeting American Society of Human Genetics, Salt Lake City, Utah. CPA 107.Al-Owain M, Iqbal M, Sakati N, Al-Hassnan Z, Teebi AS: Subteleomeric Familial
  32. 32. Rearrangement Between the Telomere of 7p and 20q Resulting in Partial Trisomy 20qter/Partial Monosomy 7pter: Clinical Phenotype and Molecular Cytogenetic Analysis. Annual Meeting American Society of Human Genetics, Salt Lake City, Utah. CPA 108.Teebi AS, Klatt R: Unilateral cleft lip and palate with hypotonia and developmental delay with duplication of NIPBL region by microarray analysis. Annual Meeting American Society of Human Genetics, Salt Lake City, Utah. PA 109.Klatt R, Teebi AS: Bannayan-Riley-Ruvalcaba Syndrome: An unusual presentation with painful vascular malformations in the extremities and Y16 X PTEN nonsense mutation. Annual Meeting American Society of Human Genetics, Salt Lake City, Utah. PA Pamphlets 1. Information for Parents. The Genetics of Syndrmic Craniosynostosis. Prepared by Ferguson M, Kennedy SJ, Teebi AS Information for Parents. Genetics of Non-Syndromic Craniosynostosis. Prepared by Ferguson M, Kennedy SJ, Teebi AS Please note 1. * - Denotes that first or second author was a student or a trainee in the Publications category. PRESENTATIONS Invited Visits to Other Hospitals/Universities/Etc. 1. Kuwait University, Faculty of Medicine, Kuwait, Jan 1990. From the genetic clinic. 2. Kuwait University, Faculty of Medicine, Kuwait, May 1990. Genetic disorders among the Arabs in Kuwait, KFAS Prize Lecture. 3. Kuwait Oil Company (KOC) Hospital, Kuwait, Jun 1990. New syndromes among the Arabs. 4. University of South Alabama, Genetic Grand Rounds, Mobile, Alabama, Oct 1990. From Bardet-Biedl to Rett. 5. Yale University, Genetic Grand Rounds, New Haven, Connecticut, Apr 1991. Malformation syndromes among the Arabs. 6. Montreal Children's Hospital & McGill University, Genetic Grand Rounds, Montreal, PQ,
  33. 33. Sep 1991. The private syndrome. 7. Alfred Dupont Institute & Nemours Children's Clinic, Pediatric Grand Rounds, Jacksonville, Florida, Mar 1992. Private and new syndromes. 8. Makkassed Hospital, Jerusalem, Nov 1992. An approach to the dysmorphic child. 9. Makkassed Hospital, Jerusalem, Nov 1992. Genetic counselling and Arabic culture, Visiting speaker. 10. Makkassed Hospital, Jerusalem, Nov 1992. Is my baby all right? (On prenatal diagnosis), Visiting speaker. 11. Makkassed Hospital, Jerusalem, Nov 1992. New developments in medical genetics. Visiting speaker. 12. Yale University, Genetic Grand Rounds, New Haven, Connecticut, Apr 1993. The concept of syndromic community. 13. Yale University, Pediatric surgery seminar, New Haven, Connecticut, May 1993. Genetics of common pediatric emergencies. 14. New York University Medical Center, Pediatric Grand Rounds, New York, Jan 1995. Dysmorphology: The history and the future. 15. Montreal Children's Hospital & McGill University, Pediatric Grand Rounds, Montreal, PQ, Feb 1995. Dysmorphology: The science and art. 16. The European Science Foundation, Conference on inherited disorders and their genes in different European populations, Barcelona, Spain, Nov 1995. Genetic disorders in The Arabs. 17. Montreal Children's Hospital & McGill University, Genetic Grand Rounds, Montreal, PQ, Feb 1996. Arab genetic diseases. 18. University of South Alabama, Part of GEN 211 course, Mobile, Alabama, Mar 1996. Mendelian inheritance and related syndromes. 19. Middle Eastern Cultural Center, Ville St. Laurent, Apr 1996. Consanguineous marriages and genetic disorders in the Arab populations. 20. Montreal Children's Hospital & McGill University, Cardiology Basic Science Conference, Montreal, PQ, May 1996. Congenital heart disease and dysmorphology. 21. David Smith Workshop on Malformations and Morphogenesis, Lake Arrowhead, California, Sep 1996. An overview on genetic and malformation syndromes among the Arabs. 22. National Center Human Genome Research, NIH, Bethesda, MD, Sep 1996. Genetic disorders among Arab populations - Genetic Seminar.
  34. 34. 23. Pediatric Grand Rounds, Saskatoon, Saskatchewan, Sep 1996. What is dysmorphology and what dysmorphology does. 24. Montreal Children's Hospital, Neonatal Rounds, Montreal, PQ, Feb 1997. Genetic aspects of congenital heart disease. 25. Hamad Medical Corporation, Qatar, Mar 1997. Dysmorphology approaches. Visiting speaker. 26. Hamad Medical Corporation, Qatar, Mar 1997. Genetic disorders among Arab populations. Visiting speaker. 27. Hamad Medical Corporation, Qatar, Mar 1997. Genetics of congenital heart disease. Visiting speaker. 28. Hamad Medical Corporation, Qatar, Mar 1997. Non-classical inheritance. Visiting speaker. 29. Hamad Medical Corporation, Qatar, Mar 1997. Recent advances in clinical genetics. Visiting speaker. 30. University of Alberta, Grand Rounds, Edmonton, Alberta, Jun 1997. Genetic disorders among the Arabs. 31. Jordan University of Science and Technology, Amman, Aug 1997. Genetic disorders among the Jordanians and Palestinians and opportunities for gene mapping. Invited Lecture. 32. Al-Quds University, Grand Rounds, Jerusalem, Aug 1997. Genetic disorders among the Palestinians. 33. 1st MEGA Conference Joint with Pasteur Institute of Tunis-Hammamet, Tunisia, Nov 1997. Genetic disease profile in the Middle-Eastern populations. 34. Abul Riche Hospital, Cairo University, Cairo, Nov 1997. Genetic diversity among the Arabs. 35. Al Demerdash Hospital, Ain Shams University, Cairo, Nov 1997. Genetic diversity among the Arabs. 36. The 1st Qatar International Pediatric Conference, Qatar, Nov 1997. Genetic Problems in Arab children from the Gulf Region. 37. Islamic Medical Association of North America meeting, Vancouver, British Columbia, Jun 1998. Genetic diversity among the Arabs. Invited speaker. 38. Abul Riche Hospital, Al Demerdash Hospital, Ain Shams University, Cairo, Egypt, Nov 1998. Grand Rounds: Genetic Diversity among the Arabs. 39. 12th. International Child Health Conference, Muscat, Oman, Feb 1999 - Mar 1999.
  35. 35. Establishing genetic services in a Gulf country. 40. 12th. International Child Health Conference, Muscat, Oman, Feb 1999 - Mar 1999. Genetic diversity among the Arabs: Lessons from the PAH & CF. Invited speaker. 41. The 2nd MEGA Conference joint with Ain Shams University, Nov 1999. Dysmorphology: The art and science. 42. The 2nd MEGA Conference joint with Ain Shams University, Nov 1999. The diversity of the Arabs: Lessons from genetic studies. 43. Al-Makkassed Hospital, Jerusalem, Dec 1999. An approach to the child with birth defects. 44. McGill University, The 5th Pancanadian Saudi Medical meeting, Montreal, PQ, Mar 2000. Role of genetics in medical practice and research. Invited speaker. 45. North York General Hospital, Genetics Rounds, Toronto, Ontario, May 2000. Dysmorphology: The science and art. 46. Ontario Dysmorphology Group, AGCO meeting, Kingston, Ontario, Jun 2000. Moderator of unknown cases session. 47. Um Al-Qurra University, Makkah, Arabia, Oct 2000. Chromosomal Syndromes. Visiting Professor. 48. Um Al-Qurra University, Makkah, Arabia, Oct 2000. Classical and non-classical inheritance. Visiting Professor. 49. The Second Arabian Gulf Medical Association Conference, Abu Dhabi, UAE, Oct 2000. Genetic counseling among Arabs. Invited speaker. 50. The Second Arabian Gulf Medical Association's Conference, Abu Dhabi, UAE, Oct 2000. Genetic disorders among Arabian Gulf populations. 51. Um Al-Qurra University, Makkah, Arabia, Oct 2000. Genetics of common birth defects. Visiting Professor. 52. Um Al-Qurra University, Makkah, Arabia, Oct 2000. Molecular diagnostics. Visiting Professor. 53. King Khalid University, Abha, Saudi Arabia, Apr 2001. Asir Pediatric Club. Dysmorphology: The Art & Science. 54. Euro-Med Gen 2001 Workshop, Tunis, Tunisia, Apr 2001. Genetic Epidemiology of The Mediterranean Population. Keynote speaker. 55. King Faisal Specialist Hospital, Jeddah, Saudi Arabia, Apr 2001. Pediatric at a Glance Symposium. Chairperson for the first session.
  36. 36. 56. King Faisal Specialist Hospital, Jeddah, Saudi Arabia, Apr 2001. Pediatric at a Glance Symposium. Genetic disorders among the Arab children. 57. King Faisal Specialist Hospital, Jeddah, Saudi Arabia, Apr 2001. Pediatric at a Glance Symposium. The dysmorphology approach. 58. King Faisal Specialist Hospital, Riyadh, Saudi Arabia, Apr 2001. Pediatric Grand Rounds. An Approach to The Dysmorphic Child. 59. King Saud University, Riyadh, Saudi Arabia, Apr 2001. Pediatric Grand Rounds. Dysmorphology: The Art & Science. 60. King Abdulaziz University, Jeddah, Saudi Arabia, Apr 2001. Pediatric Grand Rounds. Genetic disorders among the Arabs. 61. Jeddah Pediatric Club, Jeddah, Saudi Arabia, Apr 2001. What is Dysmorphology and what Dysmorphology Does. 62. Premarital Counselling Symposium, Jeddah, Saudi Arabia, Jun 2001. Chair of a session on Genetic and Metabolic diseases. 63. Premarital Counselling Symposium, Jeddah, Saudi Arabia, Jun 2001. State of Art Lecture: Genetic Diversity Among the Arabs, State of Art Lecture: Genetic Screening & Testing: The Canadian Experience. 64. Islamic Hospital, Amman, Jordan, Aug 2001. Pediatric Grand Rounds: An Approach to Birth Defects. 65. Jordan Teaching Hospital in conjunction with Jordanian Pediatrics Association, Amman, Jordan, Aug 2001. Pediatric Grand Rounds: Genetic Diversity among The Arabs: Lessons from Genetic Disease. 66. Conference on Child Health and the 9th Conference of the Union of Arab Pediatric Societies, Jeddah, Saudi Arabia, Nov 2001. Genetic Databases. 67. Conference on Child Health and the 9th Conference of the Union of Arab Pediatric Societies, Jeddah, Saudi Arabia, Nov 2001. The Dysmorphologist approach. 68. Conference on Child Health and the 9th Conference of the Union of Arab Pediatric Societies, Jeddah, Saudi Arabia, Nov 2001. Workshop: Clinical Genetics for Pediatricians with Professor Mark Gardiner. 69. Hamad Medical Corporation, Doha, Qatar, Jan 2002. An approach to the dysmorphic child. 70. Hamad Medical Corporation, Doha, Qatar, Jan 2002. Genetic Databases on and outside the Web. 71. Hamad Medical Corporation, Doha, Qatar, Jan 2002. Genetic Diversity among the Arabs.
  37. 37. 72. American College of Medical Genetics, Annual Clinical Genetics Meeting, New Orleans, Louisiana, Mar 2002. Cardinal signs and emerging genotype-phenotype association. Bartsocas Papas syndrome. 73. American College of Medical Genetics, Annual Clinical Genetics Meeting, New Orleans, Louisiana, Mar 2002. Cardinal signs and emerging genotype-phenotype association. Teebi Hypertelorism syndrome. 74. Hamad Medical Corporation, Qatar, Apr 2002. Approach to dysmorphology. 75. Um Al Qurra University, Makkah, Saudi Arabia, Apr 2002. Classical and nonclassical inheritance. Basic medical genetics, 5th year medical students. 76. Um Al Qurra University, Makkah, Saudi Arabia, Apr 2002. Clinical and Molecular Cytogenetics. Basic medical genetics, 5th year medical students. 77. Um Al Qurra University, Makkah, Saudi Arabia, Apr 2002. Clinical dysmorphology. Basic medical genetics, 5th year medical students. 78. Um Al Qurra University, Makkah, Saudi Arabia, Apr 2002. Introduction to Medical Genetics. Basic medical genetics, 5th year medical students. 79. Um Al Qurra University, Makkah, Saudi Arabia, Apr 2002. Molecular diagnostics. Basic medical genetics, 5th year medical students. 80. Um Al Qurra University, Makkah, Saudi Arabia, Apr 2002. Prenatal diagnosis. Basic medical genetics, 5th year medical students. 81. AGCO Annual Meeting, London, ON, Jun 2002. Arab Genetic Database. 82. The 10th Conference of The Union of Arab Pediatric Societies & The 9th Conference of Jordan Pediatric Society, Amman, Jordan, Oct 10, 2002. An approach to the dysmorphic child. 83. The 10th Conference of the Union of Arab Pediatric Societies and the 9th Conference of Jordan Pediatric Society, Amman, Jordan, Oct 10, 2002. Chairperson. 84. The 10th Conference of The Union of Arab Pediatric Societies & The 9th Conference of Jordan Pediatric Society, Amman, Jordan, Oct 11, 2002. Developmental delay and craniofacial anomalies. 85. Rammal Award, Euroscience, Paris, France, Dec 3, 2002. Neurodevelopment and Dysmorphology: Clues for Diagnosis. 86. Faculty of Science & Kuwait Foundation for Advancement of Science. Kuwait University, Kuwait, Dec 15, 2002. Neurodevelopment and Dysmorphology: Clues for Diagnosis. 87. Kuwait Medical Association, Kuwait, Dec 15, 2002. Neurodevelopment and Dysmorphology: Clues for Diagnosis.
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