Answer:
The chances of a hemophilic man and a female carrier having a that one of their daughters inherits the disease are 25%.
Explanation:
Since hemophilia is a disease with a sex-linked recessive inheritance pattern —X chromosome— all males who acquire the altered gene will have hemophilia ([tex]X^{h}[/tex]Y), while a female should have both altered chromosomes ([tex]X^{h}[/tex]X) to manifest the disease.
If a hemophilic male and a female carrier of the hemophilia gene have children, the possibility of having a daughter with hemophilia can be seen by crossing.
Alleles [tex]X^{h}[/tex] Y
[tex]X^{h}[/tex] [tex]X^{h}[/tex][tex]X^{h}[/tex] [tex]X^{h}[/tex]Y
X [tex]X^{h}[/tex]X XY
In the offspring, there are:
The hemophilic man and the carrier woman should know that they have a 25% chance of having a hemophilic daughter, or that 50% of their daughters may have the disease.