Approach to the Adult with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
Author:
Affiliation:
1. National Institutes of Health Clinical Center and Reproductive Biology and Medicine Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892-1932
Publisher
The Endocrine Society
Subject
Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism
Link
http://academic.oup.com/jcem/article-pdf/93/3/653/9053110/jcem0653.pdf
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3. Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from southern Germany.;Krone;J Clin Endocrinol Metab,2000
4. Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.;Speiser;J Clin Invest,1992
5. Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: implications for genetic diagnosis and association with disease manifestation.;Wedell;J Clin Endocrinol Metab,1994
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