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The Journal of Clinical Endocrinology and Metabolism|September 16, 1999
Prenatal diagnosis and treatment of 11beta-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitaliaB I Cerame, R S Newfield, L Pascoe, et al.
The Journal of Clinical Endocrinology and Metabolism|January 27, 1999
Congenital adrenal hyperplasia (21-hydroxylase deficiency) without demonstrable genetic mutationsS Nimkarn, B I Cerame, J Q Wei, et al.
American Journal of Veterinary Research|August 1, 1991
Effect of diet on gentamicin-induced nephrotoxicosis in horsesJ Schumacher, R C Wilson, J S Spano, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 14, 1999
Glucocorticoid resistance caused by reduced expression of the glucocorticoid receptor in cells from human vascular lesionsP J Bray, B Du, V M Mejia, et al.
Endocrinology|September 1, 1991
Radiotelemetric monitoring of hypothalamic gonadotropin-releasing hormone pulse generator activity throughout the menstrual cycle of the rhesus monkeyK T O'Byrne, J C Thalabard, P M Grosser, et al.
The Journal of Clinical Endocrinology and Metabolism|December 12, 2001
Prenatal diagnosis for congenital adrenal hyperplasia in 532 pregnanciesM I New, A Carlson, J Obeid, et al.
International Journal of Leprosy and Other Mycobacterial Diseases : Official Organ of the International Leprosy Association|March 1, 1989
A pilot study of three potential vaccines for leprosy in BombayR Ganapati, C R Revankar, D N Lockwood, et al.
The Journal of Steroid Biochemistry and Molecular Biology|June 1, 2001
Resistance to multiple steroids in two sistersM I New, S Nimkarn, D D Brandon, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
Resistance to several steroids in two sistersM I New, S Nimkarn, D D Brandon, et al.
The Journal of Clinical Endocrinology and Metabolism|December 13, 2003
A novel semiquantitative polymerase chain reaction/enzyme digestion-based method for detection of large scale deletions/conversions of the CYP21 gene and mutation screening in Turkish families with 21-hydroxylase deficiencyT Tukel, O Uyguner, J Q Wei, et al.
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