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3. Single-allele expression at an X-linked hyperuricemia locus in heterozygous human cells. Salzmann J; DeMars R; Benke P Proc Natl Acad Sci U S A; 1968 Jun; 60(2):545-52. PubMed ID: 5248811 [No Abstract] [Full Text] [Related]
4. Clinical features of patients with the "partial" deficiency of the X-linked uricaciduria enzyme. Greene ML Arch Intern Med; 1972 Aug; 130(2):193-8. PubMed ID: 5050554 [No Abstract] [Full Text] [Related]
5. Biochemistry of the X-linked uric aciduria--enzyme defect and its genetic variants. Kelley WN Arch Intern Med; 1972 Aug; 130(2):199-206. PubMed ID: 5050555 [No Abstract] [Full Text] [Related]
6. Studies of skin fibroblasts from 10 families with HGPRT deficiency, with reference in X-chromosomal inactivation. Migeon BR Am J Hum Genet; 1971 Mar; 23(2):199-210. PubMed ID: 5092480 [No Abstract] [Full Text] [Related]
7. X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: heterozygote has two clonal populations. Migeon BR; Der Kaloustian VM; Nyhan WL; Yough WJ; Childs B Science; 1968 Apr; 160(3826):425-7. PubMed ID: 4868511 [TBL] [Abstract][Full Text] [Related]
8. Inheritance of hypoxanthine-guanine phosphoribosyltransferase deficiency and detection of heterozygotes. Henderson JF Fed Proc; 1968; 27(4):1085-6. PubMed ID: 5658475 [No Abstract] [Full Text] [Related]
16. Genetic studies of HG- PRT deficiency and the Lesch-Nyhan syndrome with cultured human cells. DeMars R Fed Proc; 1971; 30(3):944-55. PubMed ID: 5575301 [No Abstract] [Full Text] [Related]
17. Xanthinuria in a large kindred. Wilson DM; Tapia HR Adv Exp Med Biol; 1973; 41():343-9. PubMed ID: 4791207 [No Abstract] [Full Text] [Related]
18. Clinical features of the Lesch-Nyhan syndrome. Nyhan WL Arch Intern Med; 1972 Aug; 130(2):186-92. PubMed ID: 5050553 [No Abstract] [Full Text] [Related]