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OpenStudy (anonymous):
Medals AWARDED A person with the genetic disorder Klinefelter's syndrome has an extra x-chromosome. Affected individuals have the genotype XXY. What can you infer is most likely the genetic mutation that results in Klinefelter's syndrome? Non-disjunction during meiosis Complete duplication of chromosomes during polyploidy Translocation during genetic replication Crossing over during meiosis
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OpenStudy (anonymous):
I think that it is nondisjunction, because he has an extra X due to a genetic disorder.
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