The presence of the 21-hydroxylase deficiency carrier status in hirsute women: phenotype-genotype correlations
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology,Reproductive Medicine
Reference32 articles.
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3. Identification of heterozygotic carriers of 21-hydroxylase deficiency;Witchel;Am J Med Genet,1998
4. ACTH stimulation tests and plasma dehydroepiandrosterone sulfate levels in women with hirsutism;Siegel;N Engl J Med,1990
5. Secondary biosynthetic defects in women with late-onset congenital adrenal hyperplasia;Eldar Geva;N Engl J Med,1990
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