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

Email this article to a friend

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