Just because one hypothesis may help to explain a phenomenon does not mean it is the only hypothesis that could explain it. Imag
1 answer:
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Answer:
only females
Explanation:
In humans, sex chromosomes in males and females are different. The sex chromosomes found in humans are X and Y chromosomes. X-linked trait is a trait which is inherited on the X- chromosome. According to the question, the trait is passed on a X-linked dominant condition, which means the condition is inherited on the abnormal dominant X-chromosome that will express itself even when in an heterozygous state with a normal X-chromosome.
Hence, a father affected by the condition will have a genotype; XY while a mother that does not have the condition will have a genotype: xx (two normal x chromosomes). Since the Father can only pass his X chromosome to his daughters and never his sons, all his daughters will inherit the condition (see the punnet square in attached image).
N.B: None of the sons will inherit the condition since the mother will pass normal X-chromosomes (x) to her sons.
