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Turner Syndrome occurs when an individual inherits one X chromosome but lacks a second sex
chromosome. If a phenotypically normal couple has a child with Turner syndrome that is also
color-blind (a recessive X-linked allele), did nondisjunction occur during oogenesis or
spermatogenesis in this child's parent? oogenesis Meiosis I oogenesis Meiosis II spermatogenesis
Meiosis I spermatogenesis Meiosis IIA phenotypically abnormal individual has a phenotypically
normal father with one abnormal copy of chromosome 7 and a normal mother without any
changes in chromosome structure. The order of genes along chromosome 7 in the father is as
follows: RTD M centromere PU XZC (normal 7) RTD UP centromere M XZC (abnormal 7) Use this
information for the next 2 questions. The fathers abnormal chromosome is the result of what type
of event? Pericentric inversion Paracentric inversion balanced translocation unbalanced
translocationA phenotypically abnormal individual has a phenotypically normal father with one
abnormal copy of chromosome 7 and a normal mother without any changes in chromosome
structure. The order of genes along chromosome 7 in the father is as follows: RTD M centromere
PU XZC (normal 7) RTD UP centromere M XZC (abnormal 7) The phenotypically abnormal
offspring has a chromosome 7 with the following order of genes: RTD M centromere PU DTR How
was this chromosome formed? During the the mother's gamete production, an inversion of RTD.
During the father's gamete production, a crossover between sections D and T. During the mother's
gamete production, a crossover between sections D and M. During the father's gamete
production, a crossover between centromere and section P. During the mother's gamete
production, a crossover between centromere and section P. During the the father's gamete
production, an inversion of RTD.

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Turner Syndrome occurs when an individual inherits one X chr.pdf

  • 1. Turner Syndrome occurs when an individual inherits one X chromosome but lacks a second sex chromosome. If a phenotypically normal couple has a child with Turner syndrome that is also color-blind (a recessive X-linked allele), did nondisjunction occur during oogenesis or spermatogenesis in this child's parent? oogenesis Meiosis I oogenesis Meiosis II spermatogenesis Meiosis I spermatogenesis Meiosis IIA phenotypically abnormal individual has a phenotypically normal father with one abnormal copy of chromosome 7 and a normal mother without any changes in chromosome structure. The order of genes along chromosome 7 in the father is as follows: RTD M centromere PU XZC (normal 7) RTD UP centromere M XZC (abnormal 7) Use this information for the next 2 questions. The fathers abnormal chromosome is the result of what type of event? Pericentric inversion Paracentric inversion balanced translocation unbalanced translocationA phenotypically abnormal individual has a phenotypically normal father with one abnormal copy of chromosome 7 and a normal mother without any changes in chromosome structure. The order of genes along chromosome 7 in the father is as follows: RTD M centromere PU XZC (normal 7) RTD UP centromere M XZC (abnormal 7) The phenotypically abnormal offspring has a chromosome 7 with the following order of genes: RTD M centromere PU DTR How was this chromosome formed? During the the mother's gamete production, an inversion of RTD. During the father's gamete production, a crossover between sections D and T. During the mother's gamete production, a crossover between sections D and M. During the father's gamete production, a crossover between centromere and section P. During the mother's gamete production, a crossover between centromere and section P. During the the father's gamete production, an inversion of RTD.