Associated Papers
Candidate gene analysis in a case of congenital absence of the endometrium.
Simavli S et al.
Fertility Research and Practice, 2016
Associations of Polymorphisms in WNT9B and PBX1 with Mayer-Rokitansky-Küster-Hauser Syndrome in Chinese Han.
Ma W et al.
Plos One, 2015
Mutations in HOXA11 are not responsible for Müllerian duct anomalies in Chinese patients.
Chen X et al.
Reproductive Biomedicine Online, 2014
HOXA10 and HOXA13 sequence variations in human female genital malformations including congenital absence of the uterus and vagina.
Ekici AB et al.
Gene, 2013
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