Multiple Choice
One of the rarest genome mutations, in which the affected infant has a cleft palate, abnormal heart, and developmental delays and usually does not survive beyond 6 months because of trisomy 13, is which of the following syndromes?
A) Down's
B) Turner's
C) Patau's
D) Edward's
Correct Answer:
Verified
Correct Answer:
Verified
Q1: The mutation del(15)(q11q13) on the paternal chromosome
Q3: Mutation in this gene product that catalyzes
Q4: Li-Fraumeni syndrome, in which affected patients have
Q5: Fertilization where one gamete contains an extra
Q6: Seventeen members of an extended family have
Q7: How are transmission patterns determined?<br>A) Family history<br>B)
Q8: What is indicated by the term CYP2A6?<br>A)
Q9: Mitochondrial mutations primarily affect which of the
Q10: A deceased family member is indicated in
Q11: The detection of mitochondrial mutations is complicated