Biology, asked by Fasi3363, 1 year ago

Explain the patern of inheritance of haemoplilia in humans.why is the possibility of a human female becoming haemophilic extremely rare ? explain

Answers

Answered by Nawab4381
1
Hemophilia A and hemophilia B are inherited in an X-linked recessive pattern. The genes associated with these conditions are located on the X chromosome, which is one of the two sex chromosomes. ... In X-linked recessive inheritance, a female with one altered copy of the gene in each cell is called a carrier.
Hope this is helpful for you ✌️
Similar questions