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Newborn screening compared to clinical identification of biochemical genetic disorders.
Waisbren SE, Read CY, Ampola M, Brewster TG, Demmer L, Greenstein R, Ingham CL, Korson M, Msall M, Pueschel S, Seashore M, Shih VE, Levy HL; New England Consortium of Metabolic Programs. Waisbren SE, et al. Among authors: msall m. J Inherit Metab Dis. 2002 Nov;25(7):599-600. doi: 10.1023/a:1022003726224. J Inherit Metab Dis. 2002. PMID: 12638945
237 results