Newborn screening for metabolic diseases: Saving children's lives and improving outcomes
Author:
Publisher
Elsevier BV
Subject
Clinical Biochemistry,General Medicine
Reference5 articles.
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2. Principles and practice of screening for disease;Wilson,1968
3. Rapid diagnosis of phenylketonuria by quantitative analysis of phenylalanine and tyrosine in neonatal blood spots by tandem mass spectrometry;Chace;Clin Chem,1993
4. Main report (ACMG recommendations);Watson;Genet Med,2006
5. Outcome of neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency in Australia: a cohort study;Wilcken;Lancet,2007
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