If a colourblind man marries a woman who is homozygous for normal colour vision, the probability of their son being colourblind is
$0$
$0.5$
$0.75$
$1$
A person may have one gene for normal haemoglobin and one gene for sickle cell haemoglobin. This heterozygous condition is called
Give scientific reasons : The product of phenylalanine catabolism excreted in the urine in phenylketonuria.
Which one is the incorrect statement with regard to the importance of pedigree analysis?
Sex linked disease is
A girl of normal vision whose father was colourblind marries a man of normal vision whose father was also colourblind. Their sons would be (of total number of $sons$)