Author:
Ng W. G.,Kline F.,Lin J.,Koch R.,Donnell G. N.
Subject
Genetics(clinical),Genetics
Reference33 articles.
1. Beutler, E. and Baluda, M. C. (1965). A simple spot screening test for galactosemia.J. Lab. Clin. Med.,68, 137
2. Beutler, E. and Baluda, M. C. (1966). Improved method for measuring galactose-1-phosphate uridyltransferase activity of erythrocytes.Clin. Chim. Acta,13, 369
3. Beutler, E., Baluda, M. C., Sturgeon, P. and Day, R. (1965). A new genetic abnormality resulting in galactose-1-phosphate uridyltransferase deficiency.Lancet,i, 353
4. Chacko, C. M., Christian, J. C. and Nadler, H. L. (1971). Unstable galactose-1-phosphate uridyl transferase: a new variant of galactosemia.J. Pediatr.,78, 454
5. Chacko, C. M., Wappner, R. S., Brandt, I. K. and Nadler, H. L. (1977). The Chicago variant of clinical galactosemia.Hum. Genet.,37, 261
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