Mutations in WNT4 are not responsible for Müllerian duct abnormalities in Chinese women
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Reproductive Medicine,Obstetrics and Gynecology
Reference33 articles.
1. Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky–Kuster-Hauser (MRKH) syndrome: two case reports;Bernardini;Orphanet J. Rare Dis.,2009
2. WNT4 mutation associated with Müllerian-Duct regression and virilization in a 46 XX woman;Biason;N. Engl. J. Med.,2004
3. WNT4 deficiency-a clinical phenotype distinct from the classic Mayer-Rokitansky–Kuster-Hauser syndrome: a case report;Biason;Hum. Reprod.,2007
4. Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina);Burel;J. Negat. Results Biomed.,2006
5. Report of a del22q11 in a patient with Mayer-Rokitansky–Küster–Hauser (MRKH) anomaly and exclusion of WNT-4, RAR-gamma, and RXR-alpha as major genes determining MRKH anomaly in a study of 25 affected women;Cheroki;Am. J. Med. Genet. A,2006
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1. Molecular Basis of Müllerian Agenesis Causing Congenital Uterine Factor Infertility—A Systematic Review;International Journal of Molecular Sciences;2023-12-21
2. Mutation analysis of WNT4 gene in SRY negative 46,XX DSD patients with Mullerian agenesis and/or gonadal dysgenesis- An Indian study;Gene;2023-04
3. Identification of Genetic Causes in Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome: A Systematic Review of the Literature;Children;2022-06-27
4. Analysis of copy number variations of WNT4 gene in a Chinese population with Müllerian anomalies;Orphanet Journal of Rare Diseases;2021-06-07
5. Studying Müllerian duct anomalies – from cataloguing phenotypes to discovering causation;Disease Models & Mechanisms;2021-06-01
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