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THE FLUORESCENCE IN SITU HYBRIDIZATION (FISH) ANALYSIS  IN PRADER-WILLI SYNDROME Authors: Monica Stoian, Maria Puiu, Valerica Belengeanu Department of Medical Genetics, University of Medicine and Pharmacy “Victor Babes” Timisoara, Romania
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Prader-Willi syndrome (PWS)  is a   multisystemic   disorder   caused by the loss of expression of paternally   transcribed   genes within chromosome 15q11-q13. ,[object Object],[object Object],[object Object],[object Object]
Objective ,[object Object],[object Object]
Material and method ,[object Object],[object Object],[object Object],[object Object]
Results  Cytogenetic analysis   ,[object Object],[object Object],[object Object]
[object Object]
[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],Probes
[object Object],[object Object],[object Object],Probes
[object Object],[object Object],[object Object]
[object Object],[object Object]
Technique ,[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object]
SNRPN SNRPN
SNRPN SNRPN
PWSR PWSR
SNRPN SNRPN
SNRPN SNRPN
Discussions and conclusions ,[object Object],[object Object],[object Object]
Thank you!

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