Colour blindness is
Sex-linked recessive disease
Sex-linked dominant disease
Autosomal dominant disease
Autosomal recessive disease
Among symbol $A, B$ and $C, C$ indicates
Describe Mendelian Disorder
A person may have one gene for normal haemoglobin and one gene for sickle cell haemoglobin. This heterozygous condition is called
A normalvisioned man whose father was colour blind, marries a woman whose father was also colourblind. They have their first child as a daughter. What are the chances that this child would be colour blind ?
One of the following is not true to haemophilia