1. Anderson, E. P., Kalckar, H. M., Kurahashi, K. and Isselbacher, K. J. A specific enzymatic assay for the diagnosis of congenital galactosemia. I. The consumption test.J. Lab. Clin. Med. 50 (1957) 469–477
2. Berry, G. T., Palmieri, M. J., Heals, S., Leonard, J. V. and Segal, S. Red cell uridine sugar nucleotide levels in patients with classic galactosemia.Metabolism in press
3. Beutler, E.Red Cell Metabolism. A Manual of Biochemical Methods, 3rd edn, Grune and Stratton, Orlando, FL, 1984, pp. 15–17
4. Beutler, E., West, C. and Blume, K. G. The removal of leukocytes and platelets from whole blood.J. Lab. Clin. Med. 88 (1976) 328–333
5. Frazier, D. M., Cozart, W. S. and Summer, G. K. Analysis of galactose-1-PO4 and galactose in blood by a new microfluorometric method.Biochem. Med. 20 (1978) 344–352