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
Q2: What defines a congenital disease?
A) Always heritable
B)
Q3: In a pedigree, an affected female will
Q4: Li-Fraumeni syndrome, in which affected patients have
Q5: A patient is tested to determine the
Q6: Which of the following syndromes is caused
Q8: Mitochondrial mutations primarily affect which of the
Q9: How are transmission patterns determined?
A) Family history
B)
Q10: All members of a family carry the
Q11: A patient with abnormally high iron levels
Q12: Which of the following is a genetic
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