Author:
Becroft D. M. O.,Barry D. M. J.,Webster D. R.,Simmonds H. A.
Subject
Genetics (clinical),Genetics
Reference14 articles.
1. Batshaw, M. L., Roan, Y., Jung, A. L., Rosenberg, L. A. and Brusilow, S. W. Cerebral dysfunction in asymptomatic carriers of ornithine transcarbamylase deficiency.N. Engl. J. Med. 302 (1980) 482–485
2. Campbell, A. G. M., Rosenberg, L. E., Snodgrass, P. J. and Nuzum, C. T. Ornithine transcarbamylase deficiency. A cause of lethal neonatal hyperammonemia in males.N. Engl. J. Med. 288 (1973) 1–6
3. Glasgow, A. M., Kraegel, J. H. and Schulman, J. D. Studies of the cause and treatment of hyperammonemia in females with ornithine transcarbamylase deficiency.Pediatrics 62 (1978) 30–37
4. Goldstein, A. S., Hoogenraad, N. J., Johnson, J. D., Fukanaga, K., Swierczewski, E., Cann, H. M. and Sunshine, P. Metabolic and genetic studies of a family with ornithine transcarbamylase deficiency.Pediatr. Res. 8 (1974) 5–12
5. Haan, E. A., Danks, D. M., Grimes, A. and Hoogenraad, N. J. Carrier detection in ornithine transcarbamylase deficiency.J. Inher. Metab. Dis. 5 (1982) 37–40
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