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:
i think it's true I could be wrong though
Let him have a day off and find a replacement
A tablespoon of sugar has about 48 calories.
