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