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Journal Abstract Search

251 related items for PubMed ID: 9398831

  • 1. Haemochromatosis, HFE and genetic complexity.
    Risch N.
    Nat Genet; 1997 Dec; 17(4):375-6. PubMed ID: 9398831
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  • 4. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. The European Haemochromatosis Consortium.
    Merryweather-Clarke AT, Pointon JJ, Shearman JD, Robson KJ, Jouanolle AM, Mosser A, David V, Le Gall JY, Halsall DJ, Elsey TS, Kelly A, Cox TM, Clare M, Bomford A, Vandwalle JL, Rochette J, Borot N, Coppin H, Roth MP, Ryan E, Crowe J, Totaro A, Gasparini P, Roetto A, Walker AP.
    Nat Genet; 1999 Nov; 23(3):271. PubMed ID: 10545942
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  • 5. [Clinical usefulness of the detection of mutations of the HFE gene in hemochromatosis].
    Oliva R, Sánchez M, Bruguera M, Rodés J.
    Gastroenterol Hepatol; 2000 Nov; 23(9):433-5. PubMed ID: 11126040
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  • 6. High frequency of the haemochromatosis C282Y mutation in Hungary could argue against a Celtic origin of the mutation.
    Tordai A, Andrikovics H, Kalmár L, Rajczy K, Pénzes M, Sarkadi B, Klein I, Váradi A.
    J Med Genet; 1998 Oct; 35(10):878-9. PubMed ID: 9783719
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  • 8. Human gene mutations. Gene symbol: HFE. Disease: hereditary haemochromatosis.
    de Villiers JN, Scholtz CL, Hoogendijk CF, Cawood EJ, Kotze MJ.
    Hum Genet; 1998 Jan; 102(1):127. PubMed ID: 9490291
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  • 9. Clinical haemochromatosis in HFE mutation carriers.
    Poullis A, Moodie SJ, Maxwell JD.
    Lancet; 2002 Aug 03; 360(9330):411-2; author reply 413-4. PubMed ID: 12241803
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  • 10. Haemochromatosis... definite maybe!
    Nat Genet; 1996 Aug 03; 13(4):375-6. PubMed ID: 8696321
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  • 12. [Genetic hemochromatosis and the HFE gene: from molecular genetics to clinical diagnosis].
    Höhler T, Gerken G.
    Z Gastroenterol; 2000 Jun 03; 38(6):509-15. PubMed ID: 10923364
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  • 13. Two novel polymorphisms (E277K and V212V) in the haemochromatosis gene HFE.
    Bradbury R, Fagan E, Payne SJ.
    Hum Mutat; 2000 Jan 03; 15(1):120. PubMed ID: 10612845
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  • 14. High frequency of the H63D mutation of the hemochromatosis gene (HFE) in malignant gliomas.
    Martinez di Montemuros F, Tavazzi D, Salsano E, Piepoli T, Pollo B, Fiorelli G, Finocchiaro G.
    Neurology; 2001 Oct 09; 57(7):1342. PubMed ID: 11591868
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  • 15. Overestimation of HFE C282Y homozygous hemochromatosis prevalence as the result of a common primer-binding site polymorphism.
    Press RD.
    Mol Diagn; 1999 Dec 09; 4(4):391-2. PubMed ID: 10671650
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  • 20. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.
    Noll WW, Belloni DR, Stenzel TT, Grody WW.
    Nat Genet; 1999 Nov 09; 23(3):271-2. PubMed ID: 10610176
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