What determines whether a child with a chromosome 15q11-q13 deletion will have Angelman syndrome or Prader-Willi syndrome?
A) The size of the deletion
B) The location of the 3' border of the deletion
C) The location of the 5' border of the deletion
D) The parent of origin of the deletion
E) Variation in a gene on a different chromosome
Correct Answer:
Verified
Q1: Increased sister chromatid exchange can be found
Q2: What molecular feature of the chromosome 22q11
Q3: Which of the following is the most
Q4: Which of the following is true of
Q5: Which of the following is a definite
Q6: What is the most common defect causing
Q7: Which of the following is a major
Q8: Which of the following is the most
Q9: Individuals with Klinefelter syndrome are usually infertile
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