Inborn Errors of Metabolism

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Lehmann, H. and Carrell, R.W. : Variations in the structure of human haemoglobin. Brit. Med. Bul. 25: 14, 1969.

Bcutler, E. : Glucose-6-phosphate dehydrogenase deficiency, Brit. J. Haematol , 18: 117, 1970.

Rosenberg, L.E. : Cystinuria; genetic heterogenicity and allelism . Science 154: 1341, 1966.

Jacob. F. and Monod, J. : Genetic regulatory mechanisms in the synthesis of proteins. J. Mol. Biol. 3: 318, 1961.

Parker, W.C. and Bearn, A.G. : Application of genetic regulatory mechanisms to human genetics. Amer. J. Med. 34: 680, 1963.

Auerbach, V.H. , DiGeorge, A.M. and Carpenter, G.G. : Phenylalaninemia; a study of the diversity of disorders which produce elevation of blood concentrations of phenylalanine. In Amino Acid Metabolism and Genetic Variation, Nyhan, W. L. , ed. New York, McGraw Hill , 1967, pp. 11-68.

Morrow, G. , Barness, L.A. , Cardinale, G.J. , Abeles, R.H. and Flaks, J.G. : Congenital methylmalonic acidemia; enzymatic evidence for two forms of the disease. Proc. Nat. Acad. Sci. 63: 191, 1969.

Barber, G.W. and Spaeth, G.L. : Pyridoxine therapy in homocystinuria . Lancet 1: 337, 1967.

Scriver, C.R. : Vitamin B6 deficiency and dependency in man. Amer. J. Dis. Child. 113: 109, 1967 .

Jacobson, W. : The role of pteridines in metabolic disorders . In Some Recent Advances in Inborn Errors of Metabolism. Proceedings, 4th Symposium, Society for the Study of Inborn Errors of Metabolism. Holt, K. S. and Coffey, V. P., eds. Edinburgh, Livingstone , 1968, pp. 1-13.

Mellman, W.J. : The genetic basis for the variability of heritable diseases. J. Pediat. 72: 727, 1968.

Harris, H. : Genetical theory and the inborn errors of metabolism. Brit. Med. J. 1: 321, 1970.