International perspectives on newborn screening
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/s10545-006-0259-2
Reference19 articles.
1. Autti-Rämö I, Mäkelä M, Sintonen H, et al (2005) Expanding screening for rare metabolic disease in the newborn: an analysis of costs, effect and ethical consequences of decision-making in Finland. Acta Paediatr 94:1126–1136.
2. Dionisi-Vici C, Deodato F, Röschinger W, Rhead W, Wilcken B (2006) ‘Classical’ organic acidurias, propionic aciduria, methylmalonic aciduria and isovaleric aciduria: Long-term outcome and effects of expanded newborn screening using tandem mass spectrometry. J Inherit Metab Dis 29: 383–389.
3. Green A, Pollitt RJ (1999) Population newborn screening for inherited metabolic disease: current UK perspectives. J Inherit Metab Dis 22:572–579.
4. Hall DM, Davis A (2000) Commentary on Kennedy CR, Neonatal screening for hearing impairment. Arch Dis Child 83:382–383.
5. Hall DM, Michel JM (1995) Screening in infancy. Arch Dis Child 72:93–96.
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