Answer:
The chances of a hemophilic man and a female carrier having a that one of their daughters inherits the disease are 25%.
Step-by-step 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 (
Y), while a female should have both altered chromosomes (
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.
- ♂
Y - ♀
X
Alleles
Y

Y
X
X XY
In the offspring, there are:
- Healthy sons 25%.
- Hemophilic sons 25%.
- Carrier daughters 25%.
- Hemophilic daughters 25%.
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.