Concepts of Biology
1st Edition
ISBN:9781938168116
Author:Samantha Fowler, Rebecca Roush, James Wise
Publisher:Samantha Fowler, Rebecca Roush, James Wise
Chapter7: The Cellular Basis Of Inheritance
Section: Chapter Questions
Problem 9RQ: The genotype XXY corresponds to: a. Klinefelter syndrome b. Turner syndrome c. Tripto-X d. Jacob...
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Cr-du-chat Syndrome : It is a rare genetic disorder which is caused by a missing section on a particular chromosome 5 .
Phenylketonuria : It is an autosomal recessive disorder which is caused by mutations in both alleles of the genes for phenylalanine hydroxylase , found on chromosome 12 .
Patau syndrome: It is a chromosomal abnormality in which some or all cells of the body contain extra genetic material from chromosome 13.
Fragile X syndrome : It is caused by mutation in a single gene . It turns the gene off.
Turner's syndrome : It is a condition that affects only females in which one of the X chromosome is missing or partly missing .
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