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Journal Abstract Search

152 related items for PubMed ID: 9726605

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  • 2. Role of C282Y mutation in haemochromatosis gene in development of type 2 diabetes in healthy men: prospective cohort study.
    Salonen JT, Tuomainen TP, Kontula K.
    BMJ; 2000 Jun 24; 320(7251):1706-7. PubMed ID: 10864547
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  • 3. Human gene mutations. Gene symbol: HFE. Disease: hereditary haemochromatosis.
    de Villiers JN, Scholtz CL, Hoogendijk CF, Cawood EJ, Kotze MJ.
    Hum Genet; 1998 Jan 24; 102(1):127. PubMed ID: 9490291
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  • 7. [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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  • 9. 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 08; 14(3):251-2. PubMed ID: 8896550
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  • 10. Two novel polymorphisms (E277K and V212V) in the haemochromatosis gene HFE.
    Bradbury R, Fagan E, Payne SJ.
    Hum Mutat; 2000 Jan 08; 15(1):120. PubMed ID: 10612845
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  • 11. [Detection of HFE polymorphism in German patients with hereditary hemochromatosis].
    Burggraf S, Olgemöller B.
    Dtsch Med Wochenschr; 2000 Nov 03; 125(44):1346; author reply 1347. PubMed ID: 11109419
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  • 14. Haemochromatosis: diagnosis and management after the cloning of the HFE gene.
    Powell LW, Bassett ML.
    Aust N Z J Med; 1998 Apr 03; 28(2):159-63. PubMed ID: 9612522
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  • 16. Differential HFE allele expression in hemochromatosis heterozygotes.
    Bayley JP, Verweij CL.
    Gastroenterology; 2002 Aug 03; 123(2):652-3; author reply 653. PubMed ID: 12145827
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