Newborn Screening for Inborn Errors of Metabolism
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-15720-2_3
Reference39 articles.
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2. Dussault JH, Coulombe P, Laberge C et al. (1975) Preliminary report on a mass screening program for neonatal hypothyroidism. J Pediatr 86:670–674
3. Dodge JA (1988) Implications of the new genetics for screening for cystic fibrosis. Lancet 2:672–674
4. Millington DS, Kodo N, Norwood DL, Roe CR (1990) Tandem mass spectrometry: a new method for acylcarnitine profiling with potential for neonatal screening for inborn errors of metabolism. J Inherit Metab Dis 13:321–324
5. Auray-Blais, C., Cyr, D., and Drouin, R. (2007). Quebec neonatal mass urinary screening programme: from micromolecules to macromolecules. J Inherit Metab Dis 30, 515–521.
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