Newborn screening for inborn errors of metabolism is going to expand: Are we ready?
- 30 June 1999
- journal article
- editorial
- Published by Elsevier in The Journal of Pediatrics
- Vol. 134 (6) , 666-667
- https://doi.org/10.1016/s0022-3476(99)70278-7
Abstract
No abstract availableKeywords
This publication has 3 references indexed in Scilit:
- Outcome of individuals with low-moderate methylmalonic aciduria detected through a neonatal screening programThe Journal of Pediatrics, 1999
- A systematic review of evidence for the appropriateness of neonatal screening programmes for inborn errors of metabolismJournal of Public Health, 1998
- Human Phenylalanine Hydroxylase Mutations and Hyperphenylalaninemia Phenotypes: A Metanalysis of Genotype-Phenotype CorrelationsAmerican Journal of Human Genetics, 1997