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Journal of Negative Results in BioMedicine
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Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina)

Agnès Burel, Thomas Mouchel, Sylvie Odent, Filiz Tiker, Bertrand Knebelmann, Isabelle Pellerin and Daniel Guerrier*

Journal of Negative Results in BioMedicine 2006, 5:4 doi:10.1186/1477-5751-5-4

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Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports

Laura Bernardini, Stefania Gimelli, Cristina Gervasini, Massimo Carella, Anwar Baban, Giada Frontino, Giancarlo Barbano, Maria Divizia, Luigi Fedele, Antonio Novelli, Frédérique Béna, Faustina Lalatta, Monica Miozzo, Bruno Dallapiccola Orphanet Journal of Rare Diseases 2009, 4:25 (4 November 2009)

Abstract | Full text | PDF | PubMed | Cited on BioMed Central

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Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome

Karine Morcel, Laure Camborieux, Daniel Guerrier Orphanet Journal of Rare Diseases 2007, 2:13 (14 March 2007)

Abstract | Full text | PDF | PubMed | Cited on BioMed Central

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