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Molecular Genetics and Metabolism|June 28, 2000
Fructose-1,6-diphosphatase deficiency and glyceroluria: one possible etiology for GISM E Beatty, Y H Zhang, E R McCabe, et al.
Journal of Pediatric Gastroenterology and Nutrition|February 1, 1989
Pitfalls in diagnosing galactosemia: false negative newborn screening following red blood cell transfusionR J Sokol, E R McCabe, A M Kotzer, et al.
American Journal of Human Genetics|December 1, 1992
Xp21 contiguous gene syndromes: deletion quantitation with bivariate flow karyotyping allows mapping of patient breakpointsE R McCabe, J A Towbin, G van den Engh, et al.
Child Development|December 1, 1990
Neuropsychology of early-treated phenylketonuria: specific executive function deficitsM C Welsh, B F Pennington, S Ozonoff, et al.
Biochemical Medicine and Metabolic Biology|June 1, 1991
Porin interaction with hexokinase and glycerol kinase: metabolic microcompartmentation at the outer mitochondrial membraneV Adams, L Griffin, J Towbin, 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.
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.
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