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No evidence of mutations in the genes for type I and type II 3 beta-hydroxysteroid dehydrogenase (3 beta HSD) in nonclassical 3 beta HSD deficiency.

1994; Oxford University Press; Volume: 79; Issue: 6 Linguagem: Inglês

10.1210/jcem.79.6.7989489

1945-7197

Michele Zerah, Éric Rhéaume, Puurnima Mani, Patricia Franco Cintra Schram, Jacques Simard, Fernand Labrie, Maria I. New,

Ovarian function and disorders

Journal Article No evidence of mutations in the genes for type I and type II 3 beta-hydroxysteroid dehydrogenase (3 beta HSD) in nonclassical 3 beta HSD deficiency Get access M Zerah, M Zerah 1Department of Pediatrics, New York Hospital-Cornell Medical Center, New York 10021. Search for other works by this author on: Oxford Academic Google Scholar E Rhéaume, E Rhéaume 1Department of Pediatrics, New York Hospital-Cornell Medical Center, New York 10021. Search for other works by this author on: Oxford Academic Google Scholar P Mani, P Mani 1Department of Pediatrics, New York Hospital-Cornell Medical Center, New York 10021. Search for other works by this author on: Oxford Academic Google Scholar P Schram, P Schram 1Department of Pediatrics, New York Hospital-Cornell Medical Center, New York 10021. Search for other works by this author on: Oxford Academic Google Scholar J Simard, J Simard 1Department of Pediatrics, New York Hospital-Cornell Medical Center, New York 10021. Search for other works by this author on: Oxford Academic Google Scholar F Labrie, F Labrie 1Department of Pediatrics, New York Hospital-Cornell Medical Center, New York 10021. Search for other works by this author on: Oxford Academic Google Scholar M I New M I New 1Department of Pediatrics, New York Hospital-Cornell Medical Center, New York 10021. Search for other works by this author on: Oxford Academic Google Scholar The Journal of Clinical Endocrinology & Metabolism, Volume 79, Issue 6, 1 December 1994, Pages 1811–1817, https://doi.org/10.1210/jcem.79.6.7989489 Published: 01 December 1994