Nonclassical 3β-hydroxysteroid dehydrogenase deficiency: a review of our experience with 25 female patients**Supported by United States Public Health Service, National Institutes of Health, Bethesda, Maryland, grant awards HD00072 and RR 06020. Support was also received from the United Jewish Appeal: Federation of Jewish Philantrophies of New York, Inc; and the Reichman Family Fund (Olympia and York [US] Holdings Co., New York New York).††Presented in part at the 72nd Annual Meeting of The Endocrine Society, Atlanta, Georgia, June 20 to 23, 1990.
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology,Reproductive Medicine
Reference25 articles.
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2. Four clinical variants of congenital adrenal hyperplasia;Hamilton;Arch Dis Child,1964
3. Plasma and urinary steroids in an eight year old boy with 3β-hydroxysteroid dehydrogenase deficiency;Janne;J Clin Endocrinol Metab,1970
4. Nonsalt-losing congenital adrenal hyperplasia due to 3β-hydroxy steroid dehydrogenase deficiency with normal glomerulosa function;Pang;J Clin Endocrinol Metab,1983
5. Late-onset adrenal steroid 3β-hydroxysteroid dehydrogenase deficiency. I. A cause of hirsutism in pubertal and postpubertal women;Pang;J Clin Endocrinol Metab,1985
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