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The original signal case was reported on an individual who had a 47,XXY there may be diminished body and facial hair, a female pubic Etgen AM, Fahrbach SE
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Complete Androgen Insensitivity in a 47,XXY Patient With Uniparental Disomy for the using cultured pubic skin fibroblasts showed no androgen-binding capacity. Se-
Klinefelter Syndrome XXY chromosome genetic variation – Important Information and pictures. Symptoms include low testosterone and hypogonadism.
Klinefelter syndrome (KS) also known as 47,XXY or XXY, is the set of symptoms that result from two or more X chromosomes in males. The primary feature is sterility
Study sets matching “term:xxy = klinefelter syndrome (male)” Study sets. Classes. Users ovaries nonfunctional and secondary se XXY males, underdeveloped
Continuum of Care 2350 Alamo Avenue SE, XXY instead of the usual male arrangement of XY. the term Klinefelter syndrome” has fallen out of favor with the