Suppose we have a disease phenotype that is determined by a single gene with two alleles. Further suppose it follows a autosomal recessive mode of inheritance with reduced penetrance. We have an individual who is unaffected (does not have the disease phenotype) and whose genotype is unknown. We cross this individual with a true-breeding affected individual. How many possible genotypes can this unaffected individual have at the disease locus
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Biology, 22.06.2019 02:00, rhodesnyla01
The pharynx is the structure in the body that serves as a pathway of both air and food. how does the body make sure that food does not get into the lungs? the salivary glands secrete enzymes that pull food out of the air pathway. the small intestine pushes the air out of the digestive system. the pancreas breaks down food in the air pathway. the epiglottis closes the air pathway so that food will not enter it.
Answers: 1
Biology, 22.06.2019 02:20, jimperez9616
Astudent analyzed ears of corn that demonstrated two traits in the f2 kernels, purple or white colors and smooth on wrinkled shapes. a tabulation of 135 individual kernels gave the following results: purple and smooth = 75 white and smooth = 28 purple and wrinkled = 24 white and wrinkled = 8 what would be the only phenotype present in the f1 ger
Answers: 3
Suppose we have a disease phenotype that is determined by a single gene with two alleles. Further su...
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