1. A familial disorder of uric acid metabolism and central nervous system function;Lesch, M.; Nyhan, W.L.;Amer J Med,1964
2. Enzyme defect associated with a sex-linked human neurological disorder and excessive purine synthesis;Seegmiller, J.E.; Rosenbloom, F.M.; Kelley, W.N.;Science,1967
3. Clinical syndromes associated with hypoxanthine guanine phosphoribosyl transferase deficiency;Kelley, W.N.; Wyngarden, J.D.
4. Disparate enzyme activity in erythrocytes and leukocytes;Dancis, J.; Yip, L.C.; Cox, R.P.; Piomelli, S.; Balis, M.E.;J Clin Invest,1973
5. The spectrum of hypoxanthine-guanine phosphoribosyl transferase deficiency;Emmerson, B.T.; Thompson, L.;QJ Med,1973