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Clinics in Perinatology|August 14, 2001
Postgenomic medicine. Presymptomatic testing for prediction and preventionL L McCabe, E R McCabeActa Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
State-of-the-art for DNA technology in newborn screeningE R McCabe, L L McCabeAmerican Journal of Mental Deficiency|March 1, 1985
Neuropsychological deficits in early treated phenylketonuric childrenB F Pennington, W J van Doorninck, L L McCabe, et al.Biochemical Medicine and Metabolic Biology|June 1, 1994
Application of molecular genetics in public health: improved follow-up in a neonatal hemoglobinopathy screening programY H Zhang, L L McCabe, M Wilborn, et al.Biochemical Medicine and Metabolic Biology|February 1, 1988
Blood phenylalanine estimation for the patient with phenylketonuria using a portable deviceK Peterson, R Slover, S Gass, et al.Pediatric Research|March 11, 1992
Genotypic confirmation from the original dried blood specimens in a neonatal hemoglobinopathy screening programM Descartes, Y Huang, Y H Zhang, et al.European Journal of Pediatrics|January 1, 1994
DNA techniques for screening of inborn errors of metabolismE R McCabeThe Journal of Pediatrics|April 1, 1992
Applications of DNA fingerprinting in pediatric practiceE R McCabeBiochemical Medicine|October 1, 1983
Human glycerol kinase deficiency: an inborn error of compartmental metabolismE R McCabeThe Yale Journal of Biology and Medicine|January 1, 1991
Genetic screening for the next decade: application of present and new technologiesE R McCabePageof 12