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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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