Multiple Choice
What is the most likely explanation for a set of unaffected parents having two children with a highly-penetrant, autosomal dominant disorder?
A) Two new mutations occurred in the same gene
B) Germline mosaicism in one of the parents
C) Variable expressivity
D) Somatic reversion in carrier parent
E) Inactivation of mutant allele in carrier parent
Correct Answer:
Verified
Correct Answer:
Verified
Q1: When a set of parents has a
Q2: Which type of mitochondrial mutation is NOT
Q4: Which of the following is a likely
Q5: Trinucleotide repeat alleles that are not associated
Q6: What genetic force leads to the variability
Q7: What degree of relationship to each other
Q8: For an autosomal dominant disease, if two
Q9: If an uncle has children with his
Q10: Which of the following are true about
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