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Journal Abstract Search

105 related items for PubMed ID: 18809761

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  • 2. HFE genotype and parameters of iron metabolism in German first-time blood donors - evidence for an increased transferrin saturation in C282Y heterozygotes.
    Raddatz D, Legler T, Lynen R, Addicks N, Ramadori G.
    Z Gastroenterol; 2003 Nov; 41(11):1069-76. PubMed ID: 14648375
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  • 4. A genotypic study of 217 unrelated probands diagnosed as "genetic hemochromatosis" on "classical" phenotypic criteria.
    Brissot P, Moirand R, Jouanolle AM, Guyader D, Le Gall JY, Deugnier Y, David V.
    J Hepatol; 1999 Apr; 30(4):588-93. PubMed ID: 10207799
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  • 6. Factors influencing disease phenotype and penetrance in HFE haemochromatosis.
    Rochette J, Le Gac G, Lassoued K, Férec C, Robson KJ.
    Hum Genet; 2010 Sep; 128(3):233-48. PubMed ID: 20607553
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  • 8. Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands.
    Barton JC, Sawada-Hirai R, Rothenberg BE, Acton RT.
    Blood Cells Mol Dis; 1999 Sep; 25(3-4):147-55. PubMed ID: 10575540
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  • 9. Expression of the HFE hemochromatosis gene in a community-based population of elderly women.
    Rossi E, Kuek C, Beilby JP, Jeffrey GP, Devine A, Prince RL.
    J Gastroenterol Hepatol; 2004 Oct; 19(10):1150-4. PubMed ID: 15377292
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  • 10. [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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  • 15. Mutations in HAMP and HJV genes and their impact on expression of clinical hemochromatosis in a cohort of 100 Spanish patients homozygous for the C282Y mutation of HFE gene.
    Altès A, Bach V, Ruiz A, Esteve A, Felez J, Remacha AF, Sardà MP, Baiget M.
    Ann Hematol; 2009 Oct 08; 88(10):951-5. PubMed ID: 19214511
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  • 19. The recently identified type 2A juvenile haemochromatosis gene (HJV), a second candidate modifier of the C282Y homozygous phenotype.
    Le Gac G, Scotet V, Ka C, Gourlaouen I, Bryckaert L, Jacolot S, Mura C, Férec C.
    Hum Mol Genet; 2004 Sep 01; 13(17):1913-8. PubMed ID: 15254010
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  • 20. Prevalence of C282Y and E168X HFE mutations in an Italian population of Northern European ancestry.
    Salvioni A, Mariani R, Oberkanins C, Moritz A, Mauri V, Pelucchi S, Riva A, Arosio C, Cerutti P, Piperno A.
    Haematologica; 2003 Mar 01; 88(3):250-5. PubMed ID: 12651261
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