Persistence of Müllerian derivatives and intestinal lymphangiectasis in two newborn brothers: Confirmation of the Urioste syndrome
- 2 October 2001
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 104 (1) , 69-74
- https://doi.org/10.1002/ajmg.1599
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- The Smith-Lemli-Opitz syndromeJournal of Medical Genetics, 2000
- Persistence of müllerian derivatives in malesAmerican Journal of Medical Genetics, 1999
- Persistence of müllerian derivatives, lymphangiectasis, hepatic failure, postaxial polydactyly, renal and craniofacial anomaliesAmerican Journal of Medical Genetics, 1993
- Persistent Müllerian duct remnantin a newbornUrology, 1990
- Autosomal recessive intestinal lymphangiectasia and lymphedema, with facial anomalies and mental retardationAmerican Journal of Medical Genetics, 1989
- Smith‐Lemli‐Opitz syndrome‐type II: Multiple congenital anomalies with male pseudohermaphroditism and frequent early lethalityAmerican Journal of Medical Genetics, 1987