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Which of the following mutations would be least likely to have any discernible phenotype on the individual?
A. Translocation of the last 1,000 base pairs of chromsome 1 onto chromosome 2. B. Nondisjunction of chromosome 7 to produce trisomy-7 (*2n+1) C. Nondisjunction of chromosome 8 to produce monosomy-8 (*2n-1) D. Deletion of 400 base pairs, resulting in the loss of an enhancer.
Sagot :
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