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Turner syndrome: the case of the missing sex chromosome

✍ Scribed by Andrew R. Zinn; David C. Page; Elizabeth M.C. Fisher

Book ID: 113289805
Publisher: Elsevier Science
Year: 1993
Tongue: English
Weight: 567 KB
Volume: 9
Category: Article
ISSN: 0168-9525
DOI: 10.1016/0168-9525(93)90230-f

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## Abstract Ullrich–Turner syndrome (UTS) is most commonly due to a 45,X chromosome defect, but is also seen in patients with a variety of X‐chromosome abnormalities or 45,X/46,XY mosaicism. The phenotype of UTS patients is highly variable, and depends largely on the karyotype. Patients are at an i