Generalised Dicarboxylic Aciduria: A Common Finding in Neonates
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF03335411
Reference9 articles.
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2. Anonymous. Sudden infant death and inherited metabolic disease. Lancet 2 (1986) 1073–1075
3. Bennett, M. J., Allison, F., Pollitt, R. J., Manning, N. J., Gray, R. G. F., Green, A., Hale, D. E. and Coates, P. M. Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in a family with sudden infant death. Lancet 1 (1987) 440–441
4. Bjorkman, L., McLean, C. and Steen, G. Organic acids in urine from human newborns. Clin. Chem. 22 (1976) 49–52
5. Coates, P. M., Hale, D. E., Stanley, C. A., Corkey, B. E., Hall, C. L. and Cortner, J. A. Genetic deficiency of MCAD; studies in cultured skin fibroblasts and peripheral mononuclear leukocytes. Pediatr. Res. 19 (1985) 671–676
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