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Journal Abstract Search

187 related items for PubMed ID: 9881181

  • 1. Prevalence of the C282Y mutation in Brittany: penetrance of genetic hemochromatosis?
    Jouanolle AM, Fergelot P, Raoul ML, Gandon G, Roussey M, Deugnier Y, Feingold J, Le Gall JY, David V.
    Ann Genet; 1998; 41(4):195-8. PubMed ID: 9881181
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  • 4. Frequency analysis and allele map in favor of the celtic origin of the C282Y mutation of hemochromatosis.
    Lucotte G.
    Blood Cells Mol Dis; 2001; 27(2):549-56. PubMed ID: 11500066
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  • 10. 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
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  • 13. 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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  • 15. Allele frequencies of hereditary hemochromatosis gene mutations in a local population of west Brittany.
    Jézéquel P, Bargain M, Lellouche F, Geffroy F, Dorval I.
    Hum Genet; 1998 Mar; 102(3):332-3. PubMed ID: 9544848
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  • 16. Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases.
    Sham RL, Ou CY, Cappuccio J, Braggins C, Dunnigan K, Phatak PD.
    Blood Cells Mol Dis; 1997 Aug; 23(2):314-20. PubMed ID: 9410475
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  • 17. [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
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  • 18. Nonexpressing homozygotes for C282Y hemochromatosis: minority or majority of cases?
    Adams PC.
    Mol Genet Metab; 2000 Jun; 71(1-2):81-6. PubMed ID: 11001800
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  • 19. [Hemochromatosis, a public health problem].
    Aguilar Martinez P.
    Soins; 2007 Jun; (716):34-5. PubMed ID: 17718029
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  • 20. Global prevalence of putative haemochromatosis mutations.
    Merryweather-Clarke AT, Pointon JJ, Shearman JD, Robson KJ.
    J Med Genet; 1997 Apr; 34(4):275-8. PubMed ID: 9138148
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