A girl is born with hemophilia. Her dad also has hemophilia, but her mother does not. What genetic explanation can you provide as to why the girl
suffers from hemophilia?

So daughters get 2 X chromosomes from the mom and dad and if the dad has hemophilia the daughter would get it too and sons would not get because they get Y chromosome from their dad and hemophilia is found in the X chromosome because the X chromosome is the one that has the instructions for making the clotting factor proteins.

Explanation:

A father who has hemophilia has the gene and passes it on to his daughter because daughters get two X chromosomes, one from their mother and the other from their father. This is why daughters of men with hemophilia are called obligate carriers. Since sons only receive a Y chromosome from their father, they would not have inherited hemophilia.

Hope this make sense!

answer by yourhope:

hi! : )

in which structure in the nucleus are ribosomes made?

b) nucleolus!

: )

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