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.
I think its all of the above
Answer:
Babies are made when special cells called sperm (produced by men) combine with cells called eggs (produced by women) in a process called fertilization. Each of these cells is produced by a process called meiosis which makes cells containing half the information of the parent.
Explanation:
I'm pretty sure that it's "type ll diabetes."
I believe the answer to your question will be A)
