The scenario will be Son: 25% colorblind daughter: 25% colorblind son: 25% of carrier daughters with normal vision: 25% normal son
<h3>What is color blindness?</h3>
The condition is frequently inherited. Certain eye diseases and medications are also possible causes. Men are more affected than women.
Color blindness is characterized by the inability to distinguish between red and green shades.
A colorblind man's genotype is XcY, and a heterozygous carrier female's genotype is XcX. A cross between XcY and XcX would result in progeny with the following ratio=
Son: 25% colorblind daughter: 25% colorblind son: 25% of carrier daughters with normal vision: 25% normal son.
Thus, the couple is likely to have a son who is half normal and half affected. Similarly, the couple is likely to have 50% normal daughters and 50% colorblind daughters.
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Answer:
A. The version of the trait that is expressed over other alleles for the same trait.
Explanation:
It is called dominant because if it is present, even in heterozygous situations, it will be expressed.
<span>22 pairs of autosomal chromosomes, 1 X chromosome, and 1 Y chromosome would
</span><span>be expected in a karyotype of a human male</span>
