The allele for color-blindness is carried on the X chromosome. Making color blindness (a recessive trait) an X - linked trait. A colorblind make and a carrier female for color blindness. (But is not colorblind herself) have a child. Show your work! A) what is the % chance that their son will be color blind? B) what is the % chance that their daughter will be color blind?

Please answer this quesiton.

D.     If a man is color-blind, which parent did he inherit the gene from? Explain your answer. E.     Which parent does a man get all his x-linked genes from? F.     If a woman is color-blind, what do you know about the genotypes and phenotypes of her parents?   G.     Are men more likely than women to get a genetic disease which is x-linked and dominant? Are they more likely to get a disease that is x-linked and recessive? Explain your answers.   H.    Can a man with normal color vision have a colorblind daughter? Explain your answer.   I.     Which parent determines the sex of a child?

Solve the following genetic problems involving X-linked inheritance. You must pick the right letter to represent the gene in the question. You must show your work using the Punnett square. 1 In humans, red-green colorblindness is a sex-linked recessive condition. Show a cross between a colorblind man and a woman with normal vision (homozygous normal). What are the possible phenotypes of the children? 18. Suppose a female child from the previous question grows up to marry a man with normal color vision. What are the possible genotypes and phenotypes of their children? 19. Hemophilia is a sex-linked trait where X" gives normal blood clotting and is dominant to the hemophilia allele Xh. a. Give the genotypes of 1) a woman with normal blood clotting whose father had hemophilia and 2) a normal man whose father had hemophilia.