If a mother is heterozygous (a carrier) for hemophilia and the father does not have hemophilia, each son has a 1 in 2 (50%) chance of getting his mother's hemophilia allele and having hemophilia. Each daughter has 1 in 2 (50%) chance of getting her mother's hemophilia allele and being heterozygous.
If one female is heterozygous for the hemophilia trait and is considered a carrier. One male receives a damaged X-chromosome and inherits the condition known as hemophilia. If a man does not have hemophilia, he will have a non-hemophilia allele on his X chromosome which in this case would be "H". The mans genotype would be "XHY". Man with hemophilia will have XhY genotype since it is an recessive disorder .
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