Male Pseudohermaphroditism Due to 17 β-Hydroxysteroid Dehydrogenase Deficiency (17 βHSD) in a Large Arab Kinship. Studies on the Natural History of the Defect
- 1 January 1985
- journal article
- research article
- Published by Walter de Gruyter GmbH in Journal of Pediatric Endocrinology and Metabolism
- Vol. 1 (1) , 29-38
- https://doi.org/10.1515/jpem.1985.1.1.29
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
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- Familial Male Pseudohermaphroditism with Gynecomastia Due to a Testicular 17-Ketosteroid Reductase Defect. I. Studiesin VivoJournal of Clinical Endocrinology & Metabolism, 1971