In humans, one of the genes determining color vision islocated on the X chromosome. The dominant form (C )produces normal color vision; red-green color deficiency(c) is recessive. If a man with normal color visionmarries a color-deficient woman, what is the probabilityof them having a color-deficient son? A color-deficientdaughter?

Colorblindness is an X-linked trait found in humans. What are the chances that a colorblind man will pass it on to his son? Please explain.

In humans, free ear lobes (E) is dominant over attached ear lobes (e), and brown eyes (B) is dominantover blue eyes (b). A man with free ear lobes and brown eyes marries a woman with attached ear lobes andbrown eyes. Of four children, one has free ear lobes and brown eyes, one has free ear lobes and blue eyes,one has attached ear lobes and brown eyes, and one has attached ear lobes and blue eyes. Determine thegenotypes of the parents.

Amelogenesis imperfecta (AI) is a disorder of faulty tooth enamel formation. It is inherited in an autosomal dominant and X-linked dominant pattern. The expression of AI disorder is determined by mutations in the autosomal alleles. One copy of the mutated allele (A) will cause the disorder. The severity of the disorder is determined by mutations in a gene carried on the X chromosome. Normal (or non-severe) abnormality (XN) is dominant over the abnormality (or severe) (Xn) allele. In the absence of the autosomal dominant allele, the abnormality gene on the X chromosome is not expressed. Question:A woman with normal teeth had four children with a man with non-severe form of AI: A boy was born without amelogenesis imperfecta A girl was born without amelogenesis imperfecta  A boy was born with severe amelogenesis imperfecta A boy was born with non severe amelogenesis imperfecta Identify the parental genotypes.  Complete the Punnett square for the parental cross, and identify the…