The X Chromosome.
Hemophilia occurs in the X chromosome, and males are the genders that have the X chromosome.
Hemophilia is a genetic mutation of the sex-linked X chromosome.
Hemophilia is a X linked recessive disorder. Usually the mother is an unaffected carrier and her son unfortunately receives the X chromosome in which hemophilia is linked to.
Hemophilia is a sex linked gene carried in the x chromosome.
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Because hemophilia is a disease linked to a recessive gene on the X-chromosome, females have another X-chromosome to block out the diseased one. However, males have only one X-chromosome, so they are more often subject to hemophilia.
The X chromosome. That's why it's more common in males; females have 2 X chromosomes, but males only have 1. So if a woman has the hemophilia mutation on one of her chromosomes, she probably won't be affected by it.
It is carried on the X chromosome.
It is carried on the X chromosome.
Males only have one copy of the X chromosome
Since the gene for Hemophilia is carried on the X chromosome and males pass only their Y chromosome onto their sons, no their sons should not have hemophilia. Of course all daughters of a male with hemophilia will be carriers of the mutation since they with receive his X chromosome, not the Y.
Because the gene that causes hemophilia is located on the X chromosome, so it will occur in males more frequently than in females.