Basic and clinical aspects of congenital adrenal hyperplasia
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Biochemistry
Reference36 articles.
1. Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia;Kohn;J. clin. Endocr. Metab.,1982
2. The use of cortisone in follicular phase disturbances;Jones;Fert. Steril.,1953
3. The isolation of pregnane-3,17,20-triol from the urine of women showing the adrenogenital syndrome;Butler;J. biol. Chem.,1937
4. Virilisme cliniquement tardif avec excretion de pregnanetriol et insuffisance d la production du cortisol;Decourt;Ann. Endocr.,1957
5. Radioimmunoassay of plasma 17-hydroxyprogesterone;Abraham;J. clin. Endocr. Metab.,1971
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3. A new DNA diagnostic system for the detection of human CYP21 gene mutations associated with adrenal cortex hyperplasia;Russian Journal of Bioorganic Chemistry;2010-05
4. Blood-Spot 17-Hydroxyprogesterone in Nonclassical 21-Hydroxylase Deficiency;Experimental and Clinical Endocrinology & Diabetes;2009-07-16
5. Development of Rapid and Sensitive One‐Step Direct Enzyme Linked Immunosorbent Assay for 17‐α‐OH‐Progesterone in Serum;Journal of Immunoassay and Immunochemistry;2008-03-18
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