Use of intact erythrocytes in the diagnosis of inherited purine and pyrimidine disorders
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01800045
Reference20 articles.
1. Becker, M. A., Losman, M. J. and Simmonds, H. A. Inherited PPRP synthetase superactivity due to aberrant inhibitor and activator responsiveness. In Nyhan, W. L., Thompson, L. F. and Watts, R. W. E. (eds.)Purine and Pyrimidine Metabolism in Man, 195A, Plenum, New York, 1986, pp. 59–66
2. Becroft, D. M. O., Webster, D. R., Simmonds, H. A., Fairbanks, L. D., Wilson, J. D. and Phillips, L. F. Hereditary oroticaciduria: further biochemistry. In Nyhan, W. L., Thompson, L. F. and Watts, R. W. E. (eds.)Purine and Pyrimidine Metabolism in Man, 195A, Plenum, New York, 1986, pp. 67–70
3. Cameron, J. S., Simmonds, H. A., Webster, D. R., Wass, V. and Sahota, A. Problems of diagnosis in an adolescent with hypoxanthine-guanine phosphoribosyltransferase deficiency and acute renal failure. In De Bruyn, C. H. M. M., Simmonds, H. A. and Muller, M. M. (eds.)Purine Metabolism in Man, IV-A, Plenum, New York, 1984, pp. 7–11
4. Dean, B. and Perrett, D. Studies on adenine and adenosine metabolism by intact human erythrocytes using high performance liquid chromatography.Biochim. Biophys. Acta 437 (1976) 1–15
5. Dillon, M. J., Simmonds, H. A., Barratt, T. M., Fairbanks, L. D. and Holland, P. C. Problems of diagnosis and treatment of adenine and hypoxanthine-guanine phosphoribosyltransferase deficiency in childhood. In De Bruyn, C. H. M. M., Simmonds, H. A., and Muller, M. M. (eds.)Purine Metabolism in Man, IV-A, Plenum, New York, 1984, pp. 1–6
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