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Original article
Evaluation of newborn screening for medium chain acyl-CoA dehydrogenase deficiency in 275 000 babies

Authors

  • K Carpenter aNew South Wales Newborn Screening Programme, The Children's Hospital at Westmead, Sydney, Australia, bBiochemical Genetics Service, The Children's Hospital at Westmead PubMed articlesGoogle scholar articles
  • V Wiley aNew South Wales Newborn Screening Programme, The Children's Hospital at Westmead, Sydney, Australia, bBiochemical Genetics Service, The Children's Hospital at Westmead PubMed articlesGoogle scholar articles
  • K G Sim aNew South Wales Newborn Screening Programme, The Children's Hospital at Westmead, Sydney, Australia, bBiochemical Genetics Service, The Children's Hospital at Westmead PubMed articlesGoogle scholar articles
  • D Heath aNew South Wales Newborn Screening Programme, The Children's Hospital at Westmead, Sydney, Australia, bBiochemical Genetics Service, The Children's Hospital at Westmead PubMed articlesGoogle scholar articles
  • B Wilcken aNew South Wales Newborn Screening Programme, The Children's Hospital at Westmead, Sydney, Australia, bBiochemical Genetics Service, The Children's Hospital at Westmead PubMed articlesGoogle scholar articles
  1. Dr Wilcken, The Children's Hospital at Westmead, Locked Bag 4001, Westmead, NSW 2145, AustraliaBridgetw{at}chw.edu.au
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Citation

Carpenter K, Wiley V, Sim KG, et al
Evaluation of newborn screening for medium chain acyl-CoA dehydrogenase deficiency in 275 000 babies
Archives of Disease in Childhood - Fetal and Neonatal Edition 2001;85:F105-F109.

Publication history

  • First published September 1, 2001.
Online issue publication 
January 09, 2022

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Royal College of Paediatrics and Child Health