Hey!! so I need help with a biology question if anybody can help?? 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
At vero eos et accusamus et iusto odio dignissimos ducimus qui blanditiis praesentium voluptatum deleniti atque corrupti quos dolores et quas molestias excepturi sint occaecati cupiditate non provident, similique sunt in culpa qui officia deserunt mollitia animi, id est laborum et dolorum fuga. Et harum quidem rerum facilis est et expedita distinctio. Nam libero tempore, cum soluta nobis est eligendi optio cumque nihil impedit quo minus id quod maxime placeat facere possimus, omnis voluptas assumenda est, omnis dolor repellendus. Itaque earum rerum hic tenetur a sapiente delectus, ut aut reiciendis voluptatibus maiores alias consequatur aut perferendis doloribus asperiores repellat.
I'm glad to help! What have you learned so far about each of the possible answers?
oo I have not idea about them...thats why I was hoping someone would explain them to me!! :)
Not the answer you are looking for? Search for more explanations.
Ok, I have a lesson on this let me just get the pdf...
okay thanks :)
Okay, so let's first look at what is "crossing over during meiosis" I highlighted the part that we will be looking at, but I included the full lesson in case you needed review/or didn't get to that part yet