Answer:
Option a (50%) is the correct answer.
Explanation:
- The autosomal disease does seem to be cystic fibrosis that causes the CFTR gene genetic defect. Throughout this situation, a woman, as well as a male, had already significantly impacted the child.
- Two very different parents seem to be strange alleles, which appears to mean that it would be Aa that would be heterozygous recessive. Therefore it's there's one in every biological parent again for an afflicted child throughout conception.
Other choices are not related to the given scenario. Thus, for only one of every parent, 50% of Aa.
Answer:
coronary disease, heart stroke, high blood pressure, AVC, cardiac insufficiency
Explanation:
Answer:
What type of behavior is Tina displaying
Explanation:
Just took the test
It was an international scientific research project with the goal of determining the sequence of nucleotide base pairs that make up human DNA, and of identifying and mapping all of the genes of the human genome from both a physical and a functional standpoint.
