Answer: <u>Both parents are heterozygous carriers</u>.
Explanation: Since sickle cell disease is a recessive trait, it means the affected person will have "homozygous recessive" state of genotype only. Here parents are normal, which means they are carriers. So their genotype would be Ss, heterozygous.
Heterozygous parents only will have 25% chances of having their children affected.
Option 1 is incorrect, because if one parent has two recessive alleles, it means he/she is affected and this contradicts the situation mentioned in question.
Option 3 and 4 are incorrect because it is mentioned in question that both parents are normal.
Answer:
Answer is whole-gene or whole-genome.
Explanation:
Genetic variation explains that, no matter how related or identical some organisms might be, there is a or some characters that make them different from one another. These difference is referred to as variation.
Furthermore, whole-gene means the coding and non-coding regions of the DNA>
There are some activities or occurrences that cause genetic variation, these are gene flow, mutation and sexual reproduction.
Examples of genetic variation are color of the eyes, modification of leaf and blood type among others.
Answer:
by making energy available for the cells to use
A. the cell theory stating that all living things are composed of cells.
Hope this helps!
-Payshence
Answer
Enzymes are proteins, which have a specific 3D tertiary structure, with a specifically shaped active site. The active site can only bind one substrate to form an enzyme-substrate complex, so can therefore only catalyse one reaction.