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:
Because the people you have on that list already know that you need help and will help you they know the situation so they will help and you'll know who you can count on when they are added to that list
Explanation:
A. Human error
Needs to be twenty characters so words words words words
