Colour blindness is an X-linked recessive disorder. Since males are hemizygous for chromosome, One copy of the affected gene in males in each cell is sufficient to cause the disorder (XcY ). Thus, the genotype of affected sons will be XcY. Since father transmits its X chromosome to the daughters, not to son, so the disease condition of father would not affect the disease inheritance of his son. Son receives its X chromosome from the mother which is a carrier (XcX) which means mother should carry at least one copy of affected allele to have colour blind sons. Carrier mother (XcX) transmit a normal copy of X chromosome to half of her sons and another half will get the affected copy. Thus, there will be 50% probability of sons of carrier mother to have the disease. Only colour blind mother will deliver affected X-chromosome to all of her sons. Thus, the correct answer is option A.