What is the cause of haemophilia
Chromosomal aberration
Somatic mutation
$X$-linked mutation
All the above
It's Obvious
Given is : $X$ is the chromosome with gene for haemophilia and $X$ is the chromosome with normal gene. Which of the following individuals will act as carrier for haemophilia
A colour blind son will born when
If a colour blind female marries a man whose mother was also colour blind, what are the chances of her progeny having colour blindness ?
Which of the following is not correct option for Phenylketonuria ?
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