Concept:
Colour blindness is an example of an X-linked recessive genetic disorder. The gene responsible for colour vision is located on the X chromosome.
• Males have XY chromosomes. Since they possess only one X chromosome, a single recessive allele can express the disorder.
• Females have XX chromosomes. They must inherit two recessive alleles to express colour blindness.
A carrier female has one normal allele and one recessive allele but does not show the disorder.
Given:
• Carrier female: $X^N X^c$
• Normal male: $X^N Y$
Step 1: Determine the possible gametes.
Female gametes:
\[
X^N, \; X^c
\]
Male gametes:
\[
X^N, \; Y
\]
Step 2: Construct the Punnett square for the cross.
\[
\begin{array}{c|cc}
& X^N & Y
\hline
X^N & X^N X^N & X^N Y
X^c & X^N X^c & X^c Y
\end{array}
\]
Step 3: Interpret the offspring.
• $X^N X^N$ → Normal daughter
• $X^N X^c$ → Carrier daughter
• $X^N Y$ → Normal son
• $X^c Y$ → Colour blind son
Out of the four possible offspring combinations, only one results in a colour blind son.
\[
\text{Probability} = \frac{1}{4} = 25\%
\]
Thus, the probability of a colour blind son is 25%.