<span>The light dependent reaction takes place in the fluid-filled area of a chloroplast called the stroma </span>
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
brainly.com/question/2094919
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Answer: The genotype of the child is aa
Explanation:
Both parents are normally pigmented but the child has albinism. We know that albinism is a recessive trait.
This tells us that the parents were heterozygous for albinism (Aa)
Each parent carried the recessive allele for albinism and passed it down to their child.
The parents are normally pigmented because the dominant allele (normal) masked the recessive albinism allele.
