Biology 11th Edition by Cecie Starr ,Ralph Taggart

تمرين 15

In the human population, mutation of two genes on the X chromosome causes two types of X-linked hemophilia (A and B). In a few cases, a woman is heterozygous for both mutant alleles (one on each of the X chromosomes). All of her sons should have either hemophilia A or B.
However, on very rare occasions, one of these women gives birth to a son who does not have hemophilia, and his one X chromosome does not have either mutant allele. Explain how such an X chromosome could arise.