please help on these three questions on my lab. please give clear and precise answer. thnx
1. A man and a woman are both heterozygous for a recessive allele that causes cystic fibrosis. What is the probability that their first two offspring will have the disorder?
2. When examining a human pedigree, what patterns do you look for to distinguish between X-linked recessive inheritance and autosomal recessive inheritance?
3. A woman is heterozygous for an X-linked disorder, hemophilia A. If she has a child with a man without hemophilia A, what is the sex ratio that the child will be a male with hemophilia A?