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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.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.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.[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology|November 1, 1993
[An experimental pathological study of anterior segment ischemia following recti tenotomy]Z Li, Y H ZhangPageof 82