Multiple Choice
Match the cause with the disorder.
-albinism
A) autosomal recessive inheritance resulting in abnormally low melanin levels
B) nondisjunction of the twenty-first chromosomal pair
C) X-linked recessive inheritance
D) nondisjunction of the sex chromosomes
Correct Answer:
Verified
Correct Answer:
Verified
Q22: A chromosome's gene sequence that was ABCDEFG
Q23: Figure 14.3<br> <img src="https://d2lvgg3v3hfg70.cloudfront.net/TB2278/.jpg" alt="Figure 14.3
Q24: Rarely,a chromosome's structure becomes altered when part
Q25: What is the sex chromosome composition of
Q26: Select the disorder that best matches each
Q29: In humans,which genetic mechanism led to the
Q30: If a daughter expresses an X-linked recessive
Q31: Symptoms of phenylketonuria (PKU)may be minimized or
Q32: Which nondisjunction disorder must be due to
Q58: Excerpt from Figure 14.8<br> <img src="https://d2lvgg3v3hfg70.cloudfront.net/TB2278/.jpg" alt="Excerpt