Answer: Option C
Explanation:
Color blindness is a common hereditary condition which means it usually passes from parents. Red green color blindness is passed on from the mother to the son.
The chromosome number 23 is the sex chromosome also responsible for colorblindness. As it is sex linked the son can receive the recessive allele from the mother.
The mother of the child had a recessive allele which she transferred into her son. As it is sex inherited disease the son is affected by gene carried from mother.
The correct answer is It would be more difficult for DNA to unzip since it would require more energy to break the bonds.
That is because it would most probably be a covalent bond and such a bond is stronger than a hydrogen bond which means that more energy would be needed to break it.
If mutation is associated with the centromere region, the direct impact would be on the segregating mechanism during cell division process.
"These cells cause the reabsorption of bone, thus helping to regenerate bone" is the statement that <span>is correct with respect to osteoclasts. The correct option among all the options that are given in the question is the second option or option "B". I hope the answer has helped you.</span>
