pedigree chart for colour blindness inheritance of trait , number of normal carriers and affected progeny
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To have affected progeny (affectd son and daughter) from affected male and normal female, the female should be heterozygous carrier of the trait. Since the trait is recessive, daughter can receive normal X chromosome for carrier mother and affected one from father. The resultant haterozygous daughter will be normal, though carrier. The trait under study may be colorblindness which is a X linked recessive disorder. The male parent is hemizygous recessive as human males carry one X chromosome (hemizygous) and the trait is recessive. Correct statement is A.
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