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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, Daniel Guerrier
J Negat Results Biomed. 2006; 5: 4. Published online 2006 March 23. doi: 10.1186/1477-5751-5-4
PMCID:
PMC1444933
Abstract Full Text PDF–287K

Is Cited by the Following 5 Articles in this Archive:

A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients
Katharina Rall, Gianmaria Barresi, Michael Walter, Sven Poths, Karina Haebig, Karin Schaeferhoff, Birgitt Schoenfisch, Olaf Riess, Diethelm Wallwiener, Michael Bonin, Sara Brucker
Orphanet J Rare Dis. 2011; 6: 32. Published online 2011 May 28. doi: 10.1186/1750-1172-6-32
PMCID:
PMC3123171
Abstract Full Text PDF–1.9M
Mayer-Rokitansky-Kuster-Hauser Syndrome: Surgical Management of Two Cases
I. A. Mungadi, Y. Ahmad, G. H. Yunusa, N. P. Agwu, S. Ismail
J Surg Tech Case Rep. 2010 Jan-Jun; 2(1): 39–43. doi: 10.4103/2006-8808.63725
PMCID:
PMC3214491
Abstract Full Text
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 Teresa Divizia, Luigi Fedele, Antonio Novelli, Frédérique Béna, Faustina Lalatta, Monica Miozzo, Bruno Dallapiccola
Orphanet J Rare Dis. 2009; 4: 25. Published online 2009 November 4. doi: 10.1186/1750-1172-4-25
PMCID:
PMC2777856
Abstract Full Text PDF–1.3M
Molecular analysis of the β-catenin gene in patients with the Mayer-Rokitansky-Küster-Hauser syndrome
Juliana B. Drummond, Camila F. Rezende, Fabio C. Peixoto, Joana S. Carvalho, Fernando M. Reis, Luiz De Marco
J Assist Reprod Genet. 2008 November; 25(11-12): 511–514. Published online 2008 November 1. doi: 10.1007/s10815-008-9261-y
PMCID:
PMC2593771
Abstract Full Text PDF–137K
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome
Karine Morcel, Laure Camborieux, Programme de Recherches sur les Aplasies Müllériennes (PRAM), Daniel Guerrier
Orphanet J Rare Dis. 2007; 2: 13. Published online 2007 March 14. doi: 10.1186/1750-1172-2-13
PMCID:
PMC1832178
Abstract Full Text PDF–378K
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