A colour-blind man marries a normal woman. The features of colour blindness will appear in his:

Explanation

Color blindness is a sex-linked recessive trait. This means that the gene for color blindness is located on the X chromosome. Women have two X chromosomes, while men have one X and one Y chromosome.

If a man is color blind, he has a defective X chromosome. If he marries a normal woman, she will have two normal X chromosomes. Their daughters will inherit one normal X chromosome from the mother and one defective X chromosome from the father. This means that the daughters will be carriers of the color blindness gene but will not be color blind themselves.

However, if a daughter who is a carrier has a son, there is a 50% chance that she will pass the defective X chromosome to her son. If the son inherits the defective X chromosome, he will be color blind.