Color blindness is a recessive x-linked trait in humans. In a family where the mother is color-blind, and the father is normal, the probability of their having a color-blind son is 100%.
Color blindness is a recessive x chromosome liked recessive disease which is more prone in males than in females. As the mother is color-blind she has both the alleles of colorblindness while the father is normal with both x chromosome and y chromosome normal.
So if the parents have a boy, he will always receive an x chromosome with colorblindness gene from the mother and a normal y chromosome from the father always. Thus, the probability of having a colorblind boy will be 100%.
To know more about colorblindness refer to the link below
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<span>The nitrogenous base pairs, which are linked by hydrogen bonds that also hold the strands together, are between this backbone. However, the nitrogenous bases, which are adenine, thymine, cytosine and guanine, pair up so that cytosine only pairs with guanine and adenine links up with thymine.</span>
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Unipotent stem cells are capable of differentiating into only one mature, terminally differentiated cell type. Spermatagonial stem cells are unipotent and only capable of developing into sperm cells.
Oxidative Phosphorylation: Chemiosmosis and the Electron Transport Chain
