Associated Papers
The Embryological Landscape of Mayer-Rokitansky-Kuster-Hauser Syndrome: Genetics and Environmental Factors.
Kyei-Barffour I et al.
The Yale Journal of Biology and Medicine, 2021
Case Report: A Novel Heterozygous Mutation of CD2AP in a Chinese Family With Proteinuria Leads to Focal Segmental Glomerulosclerosis.
Liu YX et al.
Frontiers in Pediatrics, 2021
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
Genetic Syndromes and Genes Involved in the Development of the Female Reproductive Tract: A Possible Role for Gene Therapy.
Connell M et al.
Journal of Genetic Syndromes & Gene Therapy, 2013
A novel mutation of HOXA10 in a Chinese woman with a Mullerian duct anomaly.
Cheng Z et al.
Human Reproduction (oxford, England), 2011
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