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Human Genetics|April 1, 1994
Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization and Southern blotP W Speiser, P C White, J Dupont, et al.Clinical Endocrinology|July 1, 1987
New findings in apparent mineralocorticoid excessJ DiMartino-Nardi, E Stoner, K Martin, et al.The Journal of Clinical Endocrinology and Metabolism|February 1, 1983
Metabolic and blood pressure responses to hydrocortisone in the syndrome of apparent mineralocorticoid excessS E Oberfield, L S Levine, R M Carey, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|March 9, 2005
The natural history and genotype-phenotype nonconcordance of HLA identical siblings with the same mutations of the 21-hydroxylase geneW Chemaitilly, B P Betensky, I Marshall, et al.Nature|November 5, 1984
Two steroid 21-hydroxylase genes are located in the murine S regionP C White, D D Chaplin, J H Weis, et al.Human Genetics|March 1, 1992
Genotype of Yupik Eskimos with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyP W Speiser, M I New, G M Tannin, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|November 11, 2005
Pregnancy outcomes in women with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiencyM Dumic, N Janjanin, J Ille, et al.Pediatric Research|December 1, 1979
Hormonal phenotype and HLA-genotype in families of patients with congenital adrenal hyperplasia (21-hydroxylase deficiency)F Lorenzen, S Pang, M I New, et al.The Journal of Clinical Endocrinology and Metabolism|January 14, 2000
Normocortisolemic Cushing's syndrome initially presenting with increased glucocorticoid receptor numbersR S Newfield, G Kalaitzoglou, T Licholai, et al.The Journal of Clinical Endocrinology and Metabolism|September 1, 1986
The syndrome of apparent mineralocorticoid excess: its association with 11 beta-dehydrogenase and 5 beta-reductase deficiency and some consequences for corticosteroid metabolismC Monder, C H Shackleton, H L Bradlow, et al.Pageof 21