Answer:
The answer is given below:
Step-by-step explanation:
Hemophilia is a sex-linked recessive disorder. The gene causing hemophilia is present on the X-chromosome. Y-chromosome does not have gene for hemophilia.
During sex determination, a daughter receives an X chromosome from her mother and an X chromosome from her father. A son gets X-chromosome from his mother and Y-chromosome from his father.
If a daughter gets haemophilic gene on X chromosome from her mother and haemophilic gene on X chromosome from her father then a daughter will be haemophilic (XhXh). Thus, in daughter hemophilia will appear only in homozygous condition.
Having heterozygous condition for haemophilic gene (xhX), the daughter is said to be carrier for hemophilia.
The son will be hemophilic if his X-chromosome has hemophilic gene ( XhY) since Y-chromosome deviod of hemeophilic gene.