Hemophilia is an X-linked recessive trait in humans. If a heterozygous woman has children with an unaffected man what is the probability of having one affected son or two unaffected
daughter?
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Explanation:
probability of son =50%
and of daughter = 50%
but probability of affected chromosome is 50%
so in probability of son getting affected is 25%
& in daughter probability of getting affected is 0%
but for being carrier it will be 25%
( father is unaffected so X normal gene will suppress the X affected gene coming from mother)
hope so... it's the easiest way by which I could explain..
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