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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.Molecular Genetics and Metabolism|May 9, 2006
Mouth cell collection device for newborn miceY-H Zhang, B-L Huang, K Eastman, et al.Child Development|August 1, 1986
Spelling errors in adults with a form of familial dyslexiaB F Pennington, L L McCabe, S D Smith, et al.Human Genetics|August 2, 2001
Glycerol kinase deficiency: evidence for complexity in a single gene disorderK M Dipple, Y H Zhang, B L Huang, et al.Human Mutation|December 19, 2001
Nine novel mutations in NR0B1 (DAX1) causing adrenal hypoplasia congenitaY H Zhang, B L Huang, K Anyane-Yeboa, et al.Pageof 1