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About Orphanet Journal of Rare Diseases
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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BioMed Central articles that cite the above article:
1.
Case Report
Hereditary renal adysplasia, pulmonary hypoplasia and Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a case report
Acién P, Galán F, Manchón I, Ruiz E, Acién M, Alcaraz LA
Orphanet Journal of Rare Diseases
2010,
5
:6
(14 April 2010)
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2.
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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