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PUBMED FOR HANDHELDS

Journal Abstract Search


199 related items for PubMed ID: 9777338

  • 1. Mutation analysis of the HLA-H gene in French hemochromatosis patients, and genetic counseling in families.
    Mercier G, Burckel A, Bathelier C, Boillat E, Lucotte G.
    Genet Couns; 1998; 9(3):181-6. PubMed ID: 9777338
    [Abstract] [Full Text] [Related]

  • 2. Frequency of the C282Y mutation of hemochromatosis in five French populations.
    Mercier G, Bathelier C, Lucotte G.
    Blood Cells Mol Dis; 1998 Jun; 24(2):165-6. PubMed ID: 9642097
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  • 3. A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations.
    Jouanolle AM, Fergelot P, Gandon G, Yaouanq J, Le Gall JY, David V.
    Hum Genet; 1997 Oct; 100(5-6):544-7. PubMed ID: 9341868
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  • 4. Celtic origin of the C282Y mutation of hemochromatosis.
    Lucotte G.
    Blood Cells Mol Dis; 1998 Dec; 24(4):433-8. PubMed ID: 9851897
    [Abstract] [Full Text] [Related]

  • 5. Hemochromatosis in Ireland and HFE.
    Ryan E, O'keane C, Crowe J.
    Blood Cells Mol Dis; 1998 Dec; 24(4):428-32. PubMed ID: 9851896
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  • 6. [Genetic hemochromatosis and the HFE gene: from molecular genetics to clinical diagnosis].
    Höhler T, Gerken G.
    Z Gastroenterol; 2000 Jun; 38(6):509-15. PubMed ID: 10923364
    [Abstract] [Full Text] [Related]

  • 7. HFE mutations analysis in 711 hemochromatosis probands: evidence for S65C implication in mild form of hemochromatosis.
    Mura C, Raguenes O, Férec C.
    Blood; 1999 Apr 15; 93(8):2502-5. PubMed ID: 10194428
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  • 11. Compound heterozygotes for hemochromatosis gene mutations: may they help to understand the pathophysiology of the disease?
    Aguilar Martinez P, Biron C, Blanc F, Masmejean C, Jeanjean P, Michel H, Schved JF.
    Blood Cells Mol Dis; 1997 Aug 15; 23(2):269-76. PubMed ID: 9410470
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  • 12. Polymorphisms in the HFE gene.
    Douabin V, Moirand R, Jouanolle A, Brissot P, Le Gall J, Deugnier Y, David V.
    Hum Hered; 1999 Jan 15; 49(1):21-6. PubMed ID: 9858853
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  • 14. A high prevalence of HLA-H 845A mutations in hemochromatosis patients and the normal population in eastern England.
    Willis G, Jennings BA, Goodman E, Fellows IW, Wimperis JZ.
    Blood Cells Mol Dis; 1997 Aug 15; 23(2):288-91. PubMed ID: 9410472
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  • 15. Mutations of the HFE gene and the risk of hepatocellular carcinoma.
    Racchi O, Mangerini R, Rapezzi D, Gaetani GF, Nobile MT, Picciotto A, Ferraris AM.
    Blood Cells Mol Dis; 1999 Aug 15; 25(5-6):350-3. PubMed ID: 10660482
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  • 18. Genetics of hemochromatosis.
    Cullen LM, Anderson GJ, Ramm GA, Jazwinska EC, Powell LW.
    Annu Rev Med; 1999 Aug 15; 50():87-98. PubMed ID: 10073265
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  • 19. 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 15; 14(3):251-2. PubMed ID: 8896550
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