Author:
Pollock M. A.,Cumberbatch M.,Bennett M. J.,Gray R. G. F.,Brand M.,Hyland K.,Congdon P. J.,Pitts-Tucker T.,Gray S.
Subject
Genetics (clinical),Genetics
Reference4 articles.
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2. Bennett, M. J., Dear, P. R. F., McGinlay, J. M. and Gray, R. G. F. Acute neonatal citrullinaemia.J. Inher. Metab. Dis. 7 (1984) 85
3. Chalmers, R. A. Organic acids in urine of patients with congenital lactic acidosis: an aid to differential diagnosis.J. Inher. Metab. Dis. 7, Suppl. 1 (1984) 79–89
4. Coudé, F. X., Ogier, H., Marsac, C., Munnich, A., Charpentier, C. and Saudubray, J. M. Secondary citrullinemia with hyperammonemia in four neonatal cases of pyruvate carboxylase deficiency.Pediatrics 68 (1981) 914
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