Brief report
Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina)
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* Corresponding author: Daniel Guerrier daniel.guerrier@univ-rennes1.fr
Journal of Negative Results in BioMedicine 2006, 5:4 doi:10.1186/1477-5751-5-4
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