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 E, Levy HL. Newborn screening compared to clinical identification of biochemical genetic disorders. Journal Of Inherited Metabolic Disease 2002, 25: 599-600. PMID: 12638945, DOI: 10.1023/a:1022003726224.Peer-Reviewed Original ResearchMeSH KeywordsAdolescentBiotinidase DeficiencyChildChild, PreschoolGalactosemiasHomocystinuriaHumansInfantInfant, NewbornMaple Syrup Urine DiseaseMetabolism, Inborn ErrorsNeonatal ScreeningOutcome Assessment, Health Care