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Journal Abstract Search

207 related items for PubMed ID: 11109419

  • 1. [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
    [No Abstract] [Full Text] [Related]

  • 2. [Detection of HFE polymorphism in German patients with hereditary hemochromatosis].
    Mensing HJ.
    Dtsch Med Wochenschr; 2000 Nov 03; 125(44):1346-7. PubMed ID: 11109420
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  • 7. [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 03; 23(9):433-5. PubMed ID: 11126040
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  • 8. HFE polymorphism and accurate diagnosis of C282Y hereditary hemochromatosis carriers.
    Elsea SH, Leykam V.
    Blood; 2000 Apr 01; 95(7):2453-5. PubMed ID: 10787240
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  • 11. Transfusion with blood from people with HFE gene mutations.
    Anía BJ, Rodríguez-Gallego C.
    Lancet; 1999 Jul 31; 354(9176):430. PubMed ID: 10437908
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  • 15. Differential HFE allele expression in hemochromatosis heterozygotes.
    Bergamaschi G, Rolandi V, Cazzola M.
    Gastroenterology; 2001 Apr 31; 120(5):1308-9. PubMed ID: 11288747
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  • 16. HFE mutation analysis in patients with hepatitis C virus with positive screening for iron overload.
    Remacha AF, Carrasco M, Sardá MP, Barceló MJ, Baiget M.
    Haematologica; 1999 Mar 31; 84(3):284-5. PubMed ID: 10189401
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  • 17. 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 31; 22(4):325-6. PubMed ID: 10431233
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