Burel, A., Mouchel, T., Odent, S., Tiker, F., Knebelmann, B., Pellerin, I., & Guerrier, D. (2006). Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina). BioMed Central.

Burel, Agnès, Thomas Mouchel, Sylvie Odent, Filiz Tiker, Bertrand Knebelmann, Isabelle Pellerin, e Daniel Guerrier. Role of HOXA7 to HOXA13 and PBX1 Genes in Various Forms of MRKH Syndrome (congenital Absence of Uterus and Vagina). BioMed Central, 2006.

Burel, Agnès, et al. Role of HOXA7 to HOXA13 and PBX1 Genes in Various Forms of MRKH Syndrome (congenital Absence of Uterus and Vagina). BioMed Central, 2006.