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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

146 related items for PubMed ID: 9418837

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  • 24. [Demonstration of HFE polymorphism in German patients with hereditary hemochromatosis].
    Erhardt A, Niederau C, Osman Y, Hassan M, Häussinger D.
    Dtsch Med Wochenschr; 1999 Dec 03; 124(48):1448-52. PubMed ID: 10615325
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  • 25. Haemochromatosis and HLA-H.
    Jazwinska EC, Cullen LM, Busfield F, Pyper WR, Webb SI, Powell LW, Morris CP, Walsh TP.
    Nat Genet; 1996 Nov 03; 14(3):249-51. PubMed ID: 8896549
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  • 29. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.
    Gomez PS, Parks S, Ries R, Tran TC, Gomez PF, Press RD.
    Nat Genet; 1999 Nov 03; 23(3):272. PubMed ID: 10545944
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  • 31. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.
    Noll WW, Belloni DR, Stenzel TT, Grody WW.
    Nat Genet; 1999 Nov 03; 23(3):271-2. PubMed ID: 10610176
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  • 32. Mutation analysis of the HLA-H gene in French hemochromatosis patients, and genetic counseling in families.
    Mercier G, Burckel A, Bathelier C, Boillat E, Lucotte G.
    Genet Couns; 1998 Nov 03; 9(3):181-6. PubMed ID: 9777338
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  • 36. Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis.
    Jeffrey GP, Chakrabarti S, Hegele RA, Adams PC.
    Nat Genet; 1999 Aug 03; 22(4):325-6. PubMed ID: 10431233
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  • 38. Human gene mutations. Gene symbol: HFE. Disease: hereditary haemochromatosis.
    de Villiers JN, Scholtz CL, Hoogendijk CF, Cawood EJ, Kotze MJ.
    Hum Genet; 1998 Jan 03; 102(1):127. PubMed ID: 9490291
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  • 39. Haemochromatosis mutation analysis in a normal Irish population.
    Ryan F, Vaughan J.
    Br J Biomed Sci; 2000 Jan 03; 57(4):315-6. PubMed ID: 11204863
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  • 40. [The prevalence of the Cys282Tyr mutation in the hemochromatosis gene in Cantabria in patients diagnosed with hereditary hemochromatosis].
    Fábrega E, Castro B, Sánchez-Castro L, Benito A, Fernández-Luna JL, Pons-Romero F.
    Med Clin (Barc); 1999 Apr 10; 112(12):451-3. PubMed ID: 10320958
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