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Science (New York, N.Y.)|May 6, 1977
H-y antigen: expression in human subjects with the testicular feminization syndromeG C Koo, S S Wachtel, P Saenger, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1995
The R337C mutation generates a high Km 11 beta-hydroxysteroid dehydrogenase type II enzyme in a family with apparent mineralocorticoid excessV R Obeyesekere, P Ferrari, R K Andrews, et al.
American Journal of Medical Genetics|October 23, 1997
Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) in CroatiaM Dumic, L Brkljacic, V Plavsic, et al.
Pediatric Research|December 14, 1999
Intrauterine growth retardation associated with maternal uniparental disomy for chromosome 6 unmasked by congenital adrenal hyperplasiaR P Spiro, S L Christian, D H Ledbetter, et al.
Hypertension (Dallas, Tex. : 1979)|January 1, 1984
Primary hyperaldosteronism in childhood due to unilateral macronodular hyperplasia. Case reportS E Oberfield, L S Levine, A Firpo, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1980
New studies of the 11 beta-hydroxylase and 18-hydroxylase enzymes in the hypertensive form of congenital adrenal hyperplasiaL S Levine, W Rauh, K Gottesdiener, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 15, 1993
Mutations in the CYP11B1 gene causing congenital adrenal hyperplasia and hypertension cluster in exons 6, 7, and 8K M Curnow, L Slutsker, J Vitek, et al.
Biochemistry|February 8, 1994
Natural mutagenesis study of the human steroid 5 alpha-reductase 2 isozymeW C Wigley, J S Prihoda, I Mowszowicz, et al.
The Journal of Clinical Endocrinology and Metabolism|June 1, 1990
Prevalence of nonclassical steroid 21-hydroxylase deficiency based on a morning salivary 17-hydroxyprogesterone screening test: a small sample studyM Zerah, H Ueshiba, E Wood, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1978
Prepubertal diagnosis of steroid 5 alpha-reductase deficiencyP Saenger, A S Goldman, L S Levine, et al.
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