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Unformatted text preview: the homozygous phenotype? If you insert a nucleotide at positions A and C, what will be the homozygous phenotype? B) If you insert a nucleotide at position A, how might you be able to suppress the mutant phenotype at position B? If you add two nucleotides at position B, name two distinct alterations you could make at position A that would suppress the phenotype. 1. 2. C) You find that you can suppress a mutation at position D by removing a nucleotide at position E, but not by removing one at position F. What does this tell you about the structure of the Fertilin gene? Tailin Fertilin...
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- Spring '09