Step-by-step explanation:
If a woman is heterozygous for Duchenne muscular dystrophy (DMD), it means that she has one normal X chromosome and one X chromosome with the DMD mutation. Since DMD is a recessive X-linked allele, the normal X chromosome will mask the effects of the DMD mutation.
When this woman has children, each child has a 50% chance of inheriting the normal X chromosome and a 50% chance of inheriting the X chromosome with the DMD mutation. Therefore, the possible outcomes for her children are:
50% chance of inheriting the normal X chromosome from the mother and a normal X chromosome from the father (XX), resulting in a normal female offspring
50% chance of inheriting the X chromosome with the DMD mutation from the mother and a normal X chromosome from the father (XDX), resulting in a female carrier of DMD.
Therefore, the percentage of females who would be heterozygous carriers of Duchenne when a woman heterozygous for DMD marries a normal man is 50%.