Author:
Page Theodore,Nyhan William L.
Reference90 articles.
1. Lesch M, Nyhan WL : A familial disorder of uric acid metabolism and central nervous system function. Am J Med 36:561–570, 1964
2. Seegmiller JE, Rosenbloom FM, Kelley WN : Enzyme defect associated with a sex-linked human neurological disorder and excessive purine synthesis. Science 155:1682–1684, 1967
3. Nyhan WL : The Lesch-Nyhan syndrome. Annu Rev Med 24:41–60, 1973
4. Gibbs DA, McFayden IR, Crawford MR, et al : First trimester diagnosis of Lesch-Nyhan syndrome. Lancet 2:1180–1183, 1984
5. Kelley WN, Wyngaarden JB : Clinical syndromes associated with hypoxanthine-guanine phosphoribosyl transferase deficiency, in Stanbury JB Wyngaarden JB Fredrickson DS, et al(eds), The Metabolic Basis of Inherited Disease, ed 5. New York, McGraw-Hill, 1983, pp 1115–1143