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Cystic fibrosis is a human disease caused by an autosomal recessive mutation. About 1 in 22 people in the human population are heterozygous carriers and have no symptoms of the disease. A woman who has a brother with CF marries a man who has no history of CF in his family. a) What are the possible genotypes of the woman? b) What is the most likely genotype of the man? c) What is the percentage of offspring that would be affected with CF, depending upon the genotype of the mother?
What is the name of the term or law that allows traits to skipa generation and appear in the next? How can we decide which monosaccharide or a disaccharide show apositive reac
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A child is born with a rare genetic disease, Tay sachs syndrome. Determine what are/is the possible combinations of phenotypesand genotypes the parents of this child will have
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