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The Journal of Clinical Endocrinology and Metabolism|November 1, 1990
Defective fasciculata zone function as the mechanism of glucocorticoid-remediable aldosteronismS Ulick, C K Chan, J R Gill, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|March 9, 2005
Update on the prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 11beta-hydroxylase deficiencyR Motaghedi, B P Betensky, B Slowinska, et al.The Journal of Clinical Endocrinology and Metabolism|March 1, 1979
6 beta-Hydroxycortisol excretion in hypercortisolemic statesE Voccia, P Saenger, R E Peterson, et al.Neurology|July 1, 1988
Preclinical Creutzfeldt-Jakob disease discovered at autopsy in a human growth hormone recipientM I New, P Brown, J W Temeck, et al.The Journal of Clinical Endocrinology and Metabolism|September 1, 1993
Defects in the HSD11 gene encoding 11 beta-hydroxysteroid dehydrogenase are not found in patients with apparent mineralocorticoid excess or 11-oxoreductase deficiencyH Nikkilä, G M Tannin, M I New, et al.The Journal of Clinical Endocrinology and Metabolism|April 1, 1983
Nonsalt-losing congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency with normal glomerulosa functionS Pang, L S Levine, E Stoner, et al.The Journal of Clinical Endocrinology and Metabolism|March 1, 1980
Hormonal studies in obligate heterozygotes and siblings of patients with 11 beta-hydroxylase deficiency congenital adrenal hyperplasiaS Pang, L S Levine, F Lorenzen, et al.Nature Genetics|July 1, 1992
Congenital adrenal hyperplasia due to point mutations in the type II 3 beta-hydroxysteroid dehydrogenase geneE Rhéaume, J Simard, Y Morel, et al.The Journal of Clinical Endocrinology and Metabolism|July 1, 1985
Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasiaS Pang, M S Pollack, M Loo, et al.The Journal of Urology|February 15, 2001
Maternal age as a risk factor for hypospadiasH Fisch, R J Golden, G L Libersen, et al.Pageof 21