A mother and father both have normal karyotypes. The father is color blind, but the mother is not. Color blindness is determined by a recessive mutation on the X chromosome. Their first child is a color-blind girl with an XX karyotype. The family consults a genetic counselor because their second child is a color blind boy with Klinefelter\'s syndrome. Klinefelter\'s syndrome results when a child has the sex chromosome constitution XXY. Which of the following statements is true about the nondisjunction event that led to the boy with Klinefelter\'s syndrome (assume no recombination)? Only during the first meiotic division in Dad. Only during the second meiotic division in Dad. Only during the first meiotic division in Mom. Only during the second meiotic division in Mom. Either a or d. Either a orb. Solution ans-e Non-disjunction (failure of homologous chromosomes) at paternal meiosis I produces XY secondary spermatocytes and a 24,XY gamete. Fertilization with a 23,X ovum produce a 47,XXY individual (Klinefelter syndrome). Only nondisjunction at paternal meiosis II produces a 24,YY gamete that yields a 47,XYY individual after fertilization..