Assume that a normal male and a female carrier of color blindness have four children: two sons and two daughters. ALL FOUR HAVE DIFFERENT GENOTYPES. The first son has normal color vision, the second son is color-blinded. The third child is a daughter and has normal color vision, but the fourth girl child is a carrier. What is the genotype of the first son, second son, the normal daughter, and the carrier daughter for color blindness? Use the the Key: A = normal color vision and dominant, a = color blind and recessive. These genes for color blindness are located on the X s*x chromosome. Y is equal to the Y chromosome.
Tags: