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.
Chicago ZitierstilBurel, Agnès, Thomas Mouchel, Sylvie Odent, Filiz Tiker, Bertrand Knebelmann, Isabelle Pellerin, und 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.
MLA ZitierstilBurel, 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.
Achtung: Diese Zitate sind unter Umständen nicht zu 100% korrekt.