MURCS association with additional congenital anomalies
Author:
Publisher
Elsevier BV
Subject
Pathology and Forensic Medicine
Reference14 articles.
1. Classification of hereditary disorders of sexual development;Wilson;Birth Defects,1975
2. The MURCS association: müllerian duct aplasia, renal aplasia, and cervicothoracic somite dysplasia;Duncan;J Pediatr,1979
3. Renal-skeletal-ear- and facial-anomalies in combination with the Mayer-Rokitansy-Kuster (MRK) syndrome;Willemsen;Eur J Obstet Gynecol Reprod Biol,1982
4. Combination of the Mayer-Rokitansky-Kuster and Klippel-Feil syndrome—a case report and literature review;Willemsen;Eur J Obstet Gynecol Reprod Biol,1982
5. Thalidomide and female genital malformations?;Hoffman;Lancet,1976
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2. Open Neural Tube Defect in a Fetus with MURCS Association: Value Addition of Fetal Autopsy in Counseling;Journal of Fetal Medicine;2020-04-10
3. Normal Embryological Development of the Female Genital Tract;Female Genital Tract Congenital Malformations;2014-12-26
4. Absence of WNT4 gene mutation in a patient with MURCS association;Journal of Pediatric Endocrinology and Metabolism;2014-01-01
5. Classification of the Female Genital Tract Malformations and its Embryological Origin. Diagnostic and Therapeutical Considerations;Current Women's Health Reviews;2013-04-01
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