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PUBMED FOR HANDHELDS

Journal Abstract Search

117 related items for PubMed ID: 10421310

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  • 2. 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; 22(4):325-6. PubMed ID: 10431233
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  • 3. Nonexpressing homozygotes for C282Y hemochromatosis: minority or majority of cases?
    Adams PC.
    Mol Genet Metab; 2000 Aug; 71(1-2):81-6. PubMed ID: 11001800
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  • 9. Molecular analysis of HLA-H gene mutations in New Zealand patients with haemochromatosis.
    Burt MJ, Upton JD, Morison IM, Chapman BA, Faed JM, George PM.
    N Z Med J; 1997 Nov 28; 110(1056):429-32. PubMed ID: 9418837
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  • 10. Hemochromatosis in Ireland and HFE.
    Ryan E, O'keane C, Crowe J.
    Blood Cells Mol Dis; 1998 Dec 28; 24(4):428-32. PubMed ID: 9851896
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  • 15. Celtic origin of the C282Y mutation of hemochromatosis.
    Lucotte G.
    Blood Cells Mol Dis; 1998 Dec 28; 24(4):433-8. PubMed ID: 9851897
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  • 16. Two novel polymorphisms (E277K and V212V) in the haemochromatosis gene HFE.
    Bradbury R, Fagan E, Payne SJ.
    Hum Mutat; 2000 Jan 28; 15(1):120. PubMed ID: 10612845
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  • 18. 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 28; 14(3):251-2. PubMed ID: 8896550
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  • 19. Longevity and carrying the C282Y mutation for haemochromatosis on the HFE gene: case control study of 492 French centenarians.
    Coppin H, Bensaid M, Fruchon S, Borot N, Blanché H, Roth MP.
    BMJ; 2003 Jul 19; 327(7407):132-3. PubMed ID: 12869454
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  • 20. 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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