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Journal Abstract Search

176 related items for PubMed ID: 12241803

  • 1. 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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  • 8. Haemochromatosis and HLA-H.
    Jouanolle AM, Gandon G, Jézéquel P, Blayau M, Campion ML, Yaouanq J, Mosser J, Fergelot P, Chauvel B, Bouric P, Carn G, Andrieux N, Gicquel I, Le Gall JY, David V.
    Nat Genet; 1996 Nov 03; 14(3):251-2. PubMed ID: 8896550
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  • 9. Genetic irony beyond haemochromatosis: clinical effects of HLA-H mutations.
    Beutler E.
    Lancet; 1997 Feb 01; 349(9048):296-7. PubMed ID: 9024367
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  • 10. Human gene mutations. Gene symbol: HFE. Disease: hereditary haemochromatosis.
    de Villiers JN, Scholtz CL, Hoogendijk CF, Cawood EJ, Kotze MJ.
    Hum Genet; 1998 Jan 01; 102(1):127. PubMed ID: 9490291
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  • 19. Role of HFE in iron metabolism, hereditary haemochromatosis, anaemia of chronic disease, and secondary iron overload.
    Townsend A, Drakesmith H.
    Lancet; 2002 Mar 02; 359(9308):786-90. PubMed ID: 11888608
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  • 20. [Frequency of HFE gene mutations and genotype-phenotype correlations in patients with hereditary hemochromatosis in Switzerland].
    Himmelmann A, Bortoluzzi L, Jansen S, Fehr J.
    Schweiz Med Wochenschr; 2000 Aug 08; 130(31-32):1112-9. PubMed ID: 11008304
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