Author:
Hösli P.,de Bruyn C. H. M. M.,Oerlemans F. J. J. M.,Verjaal M.,Nobrega R. E.
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference31 articles.
1. Boyle, J. A., Raivio, K. O., Astrin, K. H., Schulmann, J. D., Graf, M. L., Seegmiller, J. E., Jacobson, C. B.: Lesch-Nyhan syndrome: Preventive control by prenatal diagnosis. Science 169, 688?689 (1970)
2. de Bruyn, C. H. M. M.: Hypoxanthine-guanine phosphoribosyl transferase deficiency. Hum. Genet. 31, 127?150 (1976)
3. de Bruyn, C. H. M. M., Oei, T. L., Hösli, P.: Quantitative radiochemical enzyme assays in single cells: Purine phosphoribosly transferase activities in cultured fibroblasts. Biochem. Biophys. Res. Commun. 68, 483?488 (1976)
4. de Bruyn, C. H. M. M., Oei, T. L., ter Haar, B. G. A.: Studies on hairroots for carrier detection in hypoxanthine-guanine phosphoribosly transferase deficiency. Clin. Genet. 5, 449?456 (1974)
5. DeMars, R., Sarto, G., Felix, J. S., Benke, P.: Lesch-Nyhan mutation: Prenatal detection with amniotic fluid cells. Science 164, 1303?1305 (1969)
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