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A novel mutation of HOXA13 in a family with hand-foot-genital syndrome and the role of polyalanine expansions in the spectrum of Müllerian fusion anomalies

✍ Scribed by Elisa M. Jorgensen; Jane I. Ruman; Leo Doherty; Hugh S. Taylor

Book ID: 116475269
Publisher: Elsevier Science
Year: 2010
Tongue: English
Weight: 182 KB
Volume: 94
Category: Article
ISSN: 1556-5653
DOI: 10.1016/j.fertnstert.2009.05.057

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