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Newborn Screening for Primary Immunodeficiencies: Focus on Severe Combined Immunodeficiency (SCID) and Other Severe T-Cell Lymphopenias
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Neonatal Screening for Medium-Chain Acyl-CoA Dehydrogenase Deficiency—Alternative Approaches

Clinical Chemistry and Newborn Screening, The Children’s Hospital, Sheffield S10 2TH, UK
Academic Editors: Ralph Fingerhut and Peter C.J.I. Schielen
Int. J. Neonatal Screen. 2016, 2(1), 1; https://doi.org/10.3390/ijns2010001
Received: 6 February 2016 / Revised: 10 March 2016 / Accepted: 11 March 2016 / Published: 15 March 2016
The challenges inherent in many newborn screening programmes for medium-chain acyl-CoA dehydrogenase deficiency could be overcome by better use of the available second-line tests. Application of “next generation” technologies could minimize many of the problems generated by the current approach to genetic analysis. (Comment on Maier EM. Int. J. Neonatal Screen. 2015, 1, 79–88) View Full-Text
Keywords: medium-chain acyl-CoA dehydrogenase; newborn screening; neonatal screening medium-chain acyl-CoA dehydrogenase; newborn screening; neonatal screening
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Pollitt, R.J. Neonatal Screening for Medium-Chain Acyl-CoA Dehydrogenase Deficiency—Alternative Approaches. Int. J. Neonatal Screen. 2016, 2, 1.

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