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Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.
Morcel K, Camborieux L, Programme de Recherches sur les Aplasies Müllériennes , Guerrier D
Orphanet J Rare Dis 2007, 2:13
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Research
Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports
Bernardini L, Gimelli S, Gervasini C, Carella M, Baban A, Frontino G, Barbano G, Divizia MT, Fedele L, Novelli A, Béna F, Lalatta F, Miozzo M, Dallapiccola B
Orphanet Journal of Rare Diseases 2009, 4:25 (4 November 2009)
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