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American 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.Muscle & Nerve|April 1, 1989
Muscle glycerol kinase in Duchenne dystrophy and glycerol kinase deficiencyW K Seltzer, C Angelini, G Dhariwal, et al.Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|January 1, 1995
Identification of new members of a carbohydrate kinase-encoding gene familyK C Worley, K Y King, S Chua, et al.Biochemical Medicine|April 1, 1985
Adrenal dysfunction in glycerol kinase deficiencyW K Seltzer, H Firminger, J Klein, 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.Pediatrics|February 1, 1995
Amplification of bacterial DNA using highly conserved sequences: automated analysis and potential for molecular triage of sepsisK M McCabe, G Khan, Y H Zhang, et al.Science (New York, N.Y.)|January 29, 1971
ynergy of ethanol and a natural soporific--gamma hydroxybutyrateE R McCabe, E C Layne, D F Sayler, et al.Pediatrics|September 1, 1983
Newborn screening for phenylketonuria: predictive validity as a function of ageE R McCabe, L McCabe, G A Mosher, 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.American Journal of Medical Genetics|July 1, 1990
Overo lethal white foal syndrome: equine model of aganglionic megacolon (Hirschsprung disease)L McCabe, L D Griffin, A Kinzer, et al.Pageof 12