The early recognition of the 21-hydroxylase deficiency variety of congenital adrenal hyperplasia
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference24 articles.
1. Mixed adrenal disease of infancy;Knudson;J. Pediatr.,1951
2. Plasma progesterone and 17-hydroxyprogesterone in normal men and children with congenital adrenal hyperplasia;Strott;J. Clin. Invest.,1969
3. Analysis of glucocorticoid metabolites in the neonatal period: catabolism of cortisoneacetate by an infant with 21-hydroxylase deficiency;Taylor;Clin. Chim. Acta,1978
4. Variations in urinary steroid profiles after birth;Horning;Clin. Chim. Acta,1971
5. Characterization and estimation of urinary steroids of the newborn human by gas-phase analytical methods;Horning;Anal. Biochem.,1969
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