A combination of transcriptome and methylation analyses...

Orphanet Journal of Rare Diseases 2011 / 12 Vol. 6; Iss. 1

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
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Volume:
6
Language:
english
DOI:
10.1186/1750-1172-6-32
Date:
December, 2011
File:
PDF, 2.08 MB
english, 2011
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