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PUBMED FOR HANDHELDS

Journal Abstract Search


305 related items for PubMed ID: 523196

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  • 24. Genetic heterogeneity of hypoxanthine-phosphoribosyl transferase in human fibroblasts of 3 families.
    Willers I, Held KR, Singh S, Goedde HW.
    Clin Genet; 1977 Mar; 11(3):193-200. PubMed ID: 837570
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  • 28. Prenatal diagnosis of Lesch-Nyhan syndrome and some characteristics of hypoxanthine-guanine phosphoribosyltransferase and adenine phosphoribosyltransferase in human tissues and cultivated cells.
    Shin-Buehring YS, Osang M, Wirtz A, Haas B, Rahm P, Schaub J.
    Pediatr Res; 1980 Jun; 14(6):825-9. PubMed ID: 7402756
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  • 33. Purine metabolism in normal and thioguanine-resistant neuroblastoma.
    Wood AW, Becker MA, Minna JD, Seegmiller JE.
    Proc Natl Acad Sci U S A; 1973 Dec; 70(12):3880-3. PubMed ID: 4521214
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  • 34. Genetic analysis of the HPRT mutation of Lesch-Nyhan syndrome in a Chinese family.
    Lee WJ, Lee HM, Chi CS, Yang MT, Lin HY, Lin WH.
    Zhonghua Yi Xue Za Zhi (Taipei); 1995 Dec; 56(6):359-66. PubMed ID: 8851475
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  • 36. Lesch-Nyhan syndrome: biochemical characterization of a case with attenuated behavioral manifestation.
    Fattal A, Spirer Z, Zoref-Shani E, Sperling O.
    Enzyme; 1984 Dec; 31(1):55-60. PubMed ID: 6201351
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  • 37. Impaired differentiation of HPRT-deficient dopaminergic neurons: a possible mechanism underlying neuronal dysfunction in Lesch-Nyhan syndrome.
    Yeh J, Zheng S, Howard BD.
    J Neurosci Res; 1998 Jul 01; 53(1):78-85. PubMed ID: 9670994
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