Colour blindness in man is
Due of deficiency of vitamin $A$
Due of absence of visual purple in retina
Due to absence of rods in retina
A sex linked abnormality
It's Obvious
A boy is colour blind, in his two sisters one is colour blind and one is carrier $(normal)$. Then who is colour blind in his family
Disorder inherited as Mendel's law of inheritance called
Colour blindness is caused by a single
A woman with normal vision, but whose father was colour blind, marries a colour blind man. Suppose that the fourth child of this couple was a boy. Thus boy
If a character is always transmitted directly from a father to all his sons and from their sons to all their sons, then which chromosome carries the gene for the character
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