Detection of 3β-hydroxysteroid dehydrogenase deficiency in a newborn by means of urinary steroid analysis
Author:
Publisher
Elsevier BV
Subject
Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine
Reference13 articles.
1. Neonatal screening programme for congenital adrenal hyperplasia in a homogenous Caucasian population;Cacciari;J Inher Metab Dis,1986
2. Clinical aspects of congenital adrenal hyperplasia: early diagnosis and prognosis;Hughes;J Inher Metab Dis,1986
3. Biochemical aspects of congenital adrenal hyperplasia;Honour;J Inher Metab Dis,1986
4. The early recognition of the 21-hydroxylase deficiency variety of congenital adrenal hyperplasia;Steen;Clin Chim Acta,1980
5. An atlas of gas chromatographic profiles of neutral urinary steroids in health and disease;Schackleton,1980
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