A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients

A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients

<p>Abstract</p> <p>Background</p> <p>The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is present in at least 1 out of 4,500 female live births and is the second most common cause for primary amenorrhea. It is characterized by vaginal and uterine aplasia in an XX indiv...

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Bibliographic Details
Main Authors: Riess Olaf, Schoenfisch Birgitt, Schaeferhoff Karin, Haebig Karina, Poths Sven, Walter Michael, Barresi Gianmaria, Rall Katharina, Wallwiener Diethelm, Bonin Michael, Brucker Sara
Format: Article
Language:English
Published: BMC 2011-05-01
Series:Orphanet Journal of Rare Diseases
Online Access:http://www.ojrd.com/content/6/1/32

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http://www.ojrd.com/content/6/1/32

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