Answer:
can you please provide the name of this leaf...
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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DNA I’m not sure if im right sorry if im wrong
Answer:
for number one i got ☐ It involves the modification of DNA
☐ It attempts to replace a mutated gene with normal DNA.
☐ It does not always cure patients who use it.
FOR NUMBER TWO I GOT:
D.)genotype: Rr
phenotype: black eyes
plz mark brainliest!!!
