Neonatal Screening for 21-Hydroxylase Deficient Congenital Adrenal Hyperplasia--The Role of CYP21 Analysis
Author:
Publisher
The Endocrine Society
Subject
Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Children with premature pubarche: is an alterated neonatal 17-Ohp screening test a predictive factor?;Italian Journal of Pediatrics;2018-01-16
2. Neonatal screening for congenital adrenal hyperplasia: transitory elevation of 17-hydroxyprogesterone;Journal of Pediatric Endocrinology and Metabolism;2011-01-01
3. Transient hyper-17-hydroxyprogesteronemia: a clinical subgroup of patients diagnosed at neonatal screening for congenital adrenal hyperplasia;European Journal of Endocrinology;2009-08
4. Using real-time, quantitative PCR for rapid genotyping of the steroid 21-hydroxylase gene in a north Florida population;J CLIN ENDOCR METAB;2002
5. Newborn Screening for Congenital Adrenal Hyperplasia inthe Netherlands;Pediatrics;2001-12-01
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