Molecular genetics of congenital adrenal hyperplasia (21-hydroxylase deficiency): implications for diagnosis, prognosis and treatment
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.1998.tb00968.x/fullpdf
Reference30 articles.
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2. Congenital adrenal hyperplasia;White;N Engl J Med,1987
3. Microfilter paper method for 17-hydroxyprogesterone radioimmunoassay; its application for rapid screening for congenital adrenal hyperplasia;Pang;J Clin Endocrinol Metab,1977
4. Congenital adrenal hyperplasia due to 21-hydroxy-lase deficiency: Newborn screening and its relationship to the diagnosis and treatment of the disorder;Pang;Screening,1993
5. High frequency of nonclassical steroid 21-hydroxylase deficiency;Speiser;Am J Hum Genet,1985
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