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Journal Abstract Search

240 related items for PubMed ID: 7448460

  • 21. Inherited deficiency of hypoxanthine-guanine phosphoribosyltransferase in X-linked uric aciduria (the Lesch-Nyhan syndrome and its variants).
    Seegmiller JE.
    Adv Hum Genet; 1976; 6():75-163. PubMed ID: 779428
    [No Abstract] [Full Text] [Related]

  • 22. Clinical correlations in partial hypoxanthine guanine phosphoribosyltransferase deficiency.
    Hersh JH, Page T, Hand ME, Seegmiller JE, Nyhan WL, Weisskopf B.
    Pediatr Neurol; 1986; 2(5):302-4. PubMed ID: 3508703
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  • 23. Urate kinetics in hypoxanthine-guanine phosphoribosyltransferase deficiency: their significance for the understanding of gout.
    Emmerson BT, Gordon RB, Johnson LA.
    Q J Med; 1976 Jan; 45(177):49-61. PubMed ID: 769040
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  • 24. Lesch-Nyhan syndrome. Repository identification Nos. GM-2290, 2291, 2292, 2338, 3115, 3116, and 3117.
    Tischfield J, Schafer IA, Dickerman LH, Trill J, Mulivor RA, Greene AE, Coriell LL.
    Cytogenet Cell Genet; 1979 Jan; 24(3):199-200. PubMed ID: 477417
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  • 31. Production of a model for Lesch-Nyhan syndrome in hypoxanthine phosphoribosyltransferase-deficient mice.
    Wu CL, Melton DW.
    Nat Genet; 1993 Mar; 3(3):235-40. PubMed ID: 8485579
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  • 32. [Lesch-Nyhan syndrome].
    Akaoka I.
    Nihon Rinsho; 1975 Feb 10; 33(2):340-4. PubMed ID: 1170375
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  • 33. Normal HPRT coding region in a male with gout due to HPRT deficiency.
    Dawson PA, Gordon RB, Keough DT, Emmerson BT.
    Mol Genet Metab; 2005 May 10; 85(1):78-80. PubMed ID: 15862284
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  • 34. Molecular genetics of the HPRT-deficiency syndromes.
    Wilson JM, Kelley WN.
    Hosp Pract (Off Ed); 1984 May 10; 19(5):81-9, 93-7, 100. PubMed ID: 6425346
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