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- Jul 6, 2015
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Please take a look at this question and explain how a boy can have both hemophilia and color blindness (which are unlinked genes on different x chromosomes). I was under the impression that the boy would get a Y chromosome from the father with no disease... and now the mother passes down one of her X chromosomes to him with EITHER hemophilia or colorblindness. If the mother has one X (hemophilia) and one X (colorblindness) she can only pass down one or the other to this boy? This probability renders to me as 0%. Can someone clarify.
Bootcamp test 2 question...
Bootcamp test 2 question...