In a human,what is the best explanation for being XX and phenotypically male?
A) One of the X's is incomplete resembling a chromosome. B) A small piece of the Y-chromosome, containing the SRY region, is inserted on the X-chromosome. C) Both the X's have a mutation deleting the "female" forming genes. D) There is a fragment of the Y-chromosome inserted on an autosomal chromosome. E) The SRY gene has mutated.