REFERENCES
- Garrod, A. E.: Inborn Errors of Metabolism. Ed. 2. London, Oxford University Press, 1923.
- LeLoir, L. F.: Metabolism of hexosephosphates. In McElroy, W. D. and Glass, B.: Phosphorus Metabolism. Baltimore, Maryland, The Johns Hopkins Press, 1951, vol. 1, p. 67.
- Schwarz, V., Goldberg, L., Komrower, G. M. and Holzel, A.: Some disturbances of erythrocyte metabolism in galactosemia. Biochem. J. 62:34 (January) 1956.
- Isselbacher, K. J., Anderson, E. P., Kurahashi, K. and Kalckar, H. M.: Congenital galactosemia, a single enzymatic block in galactose metabolism. Science 123:635 (April 13) 1956.
- Hsia, D. Y. Y., Driscoll, K., Troll, W. and Knox, W. E.: Heterozygote carriers of phenylketonuria detected by phenylalanine tolerance tests. Nature 178:1239 (December) 1956.
- Hsia, D. Y. Y.: The laboratory detection of heterozygotes. Am. J. Human Genet. (In press.)
- Lawler, S. D. and Sandler, M.: Data on linkage in man: Elliptocytosis and blood groups. IV. Families 5, 6 and 7. Ann. Human Genet. 18:328 (March) 1954.
- Bickel, H., Gerrard, J. and Hickmans, E. M.: Influence of phenylalanine intake on phenylketonuria. Lancet 2:812 (October 17) 1953.
- Hsia, D. Y. Y., Paine, R. C. and Knox, W. E.: Unpublished data.