A phenotypically normal man's grandfather had galactosemia, a rare autosomal recessive disease caused by the inability to process galactose. Assume that the man's only possible source of the mutant allele for galactosemia is from his grandfather. This man marries a phenotypically normal woman who has phenotypically normal parents, but does have a sister with galactosemia. What is the probability that their first child will be a boy and will have galactosemia

Awoman whose sister tested positive for a specific mutation in the brca1 gene, which increases the risk for breast and ovarian cancer, is found not to have that mutation but does have a mutation of unknown significance near the known mutation site. how should this woman be counseled? select one: a. she should be informed that her risk for breast cancer is greater than the general population but not as great as her sister’s risk. b. she should be informed that because she does not have the mutation, her risk for breast cancer is not greater than that of the general population. c. she should be informed of her gene mutation status and be presented with all the available prophylaxis options and reconstruction options. d. she should be informed that she does not have the specific mutation but that because another mutation is present she should be vigilant about screening