Colorblindness is an X linked gene. Normal vision (XN ) is dominant over colorblind (Xn). Cross a carrier female to a normal male. How many of their children will be colorblind? How many of their sons will be colorblind? How many of their daughters will be colorblind?

The most common form of colorblindness is a recessive, sex-linked hereditary con dition caused by a defect on the X chromosome. Females are XX, while males are XY. Individuals inherit one chromosome from each parent, with equal probability; for example, an individual has a 50% chance of inheriting their father's X chromosome, and a 50% chance of inheriting their father's Y chromosome. If a male has an X chromosome with the defect, he is colorblind. However, a female with only one defective X chromo some will not be colorblind. Thus, colorblindness is more common in males than females; 7% of males are colorblind but only 0.5% of females are colorblind. (a) Assume that the X chromosome with the wild-type allele is X+ and the one with the disease allele is X. What is the expected frequency of each possible female genotype: X+X+, X+X¯, and X-X-? What is the expected frequency of each possible male genotype: X+ Y and X-Y? (b) Suppose that two parents are not colorblind. What is the…

Mary and Ron don't have albinism. However, is it possible for them to have a child with albinism? Explain. Stephanie has normal color vision. Her husband Chris also has normal color vision. They have a son that is color blind and a daughter that has normal color vision. What is the genotype of the mother, father, son and the daughter? Andy and Anne do not have polydactyl. Is it possible for them to have a child with polydactyl? Explain. When examining a pedigree chart, I notice that only males are affected. What does this tell me about the inheritance pattern? A man with blood type A marries a woman with blood type B. Their child has blood type O. What are the genotypes of the parents?