17β-hydroxysteroid dehydrogenase 3 deficiency in a male pseudohermaphrodite
- 31 January 2008
- journal article
- case report
- Published by Elsevier BV in Fertility and Sterility
- Vol. 89 (1), 228.e13-228.e17
- https://doi.org/10.1016/j.fertnstert.2007.02.048
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Substitution Mutation C268Y Causes 17 -Hydroxysteroid Dehydrogenase 3 DeficiencyJournal of Clinical Endocrinology & Metabolism, 2001
- Male Pseudohermaphroditism due to 17β-Hydroxysteroid Dehydrogenase 3 Deficiency: Diagnosis, Psychological Evaluation, and ManagementMedicine, 2000
- 17 -Hydroxysteroid Dehydrogenase-3 Deficiency: Diagnosis, Phenotypic Variability, Population Genetics, and Worldwide Distribution of Ancient and de Novo MutationsJournal of Clinical Endocrinology & Metabolism, 1999
- Deleterious Missense Mutations and Silent Polymorphism in the Human 17 -Hydroxysteroid Dehydrogenase 3 Gene (HSD17B3)Journal of Clinical Endocrinology & Metabolism, 1998
- The Identification of 5 -Reductase-2 and 17 -Hydroxysteroid Dehydrogenase-3 Gene Defects in Male Pseudohermaphrodites from a Turkish KindredJournal of Clinical Endocrinology & Metabolism, 1998
- Physiology and molecular genetics of 17β-hydroxysteroid dehydrogenasesSteroids, 1997
- Molecular genetics and pathophysiology of 17 beta-hydroxysteroid dehydrogenase 3 deficiencyJournal of Clinical Endocrinology & Metabolism, 1996
- Male pseudohermaphroditism caused by mutations of testicular 17β–hydroxysteroid dehydrogenase 3Nature Genetics, 1994
- Mechanisms of androgen production in male pseudohermaphroditism due to 17 beta-hydroxysteroid dehydrogenase deficiencyJournal of Clinical Endocrinology & Metabolism, 1992
- Male pseudohermaphroditism: The complexities of male phenotypic developmentAmerican Journal Of Medicine, 1976