Author:
Bennett M. J.,Coates P. M.,Hale D. E.,Millington D. S.,Pollitt R. J.,Rinaldo P.,Roe C. R.,Tanaka K.
Subject
Genetics(clinical),Genetics
Reference21 articles.
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3. Bennett, M. J., Worthy, E. and Pollitt, R. J. The incidence and presentation of dicarboxylic aciduria.J. Inher. Metab. Dis. 10 (1987b) 241–241
4. Bennett, M. J., Allison, F., Pollitt, R. J. and Variend, S. Fatty acid oxidation defects as causes of unexpected death in infancy. In Tanaka, K. and Coates, P. M. (eds.),Fatty Acid Oxidation: Clinical, Biochemical and Molecular Aspects, Liss, New York, 1989, pp. 349–364
5. Coates, P. M., Hale, D. E., Stanley, C. A., Corkey, B. E. and Cortner, J. A. Genetic deficiency of medium-chain acyl-CoA dehydrogenase: studies in cultured skin fibroblasts and peripheral mononuclear leukocytes.Pediatr. Res. 19 (1985) 671–676
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