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Journal Abstract Search

251 related items for PubMed ID: 26501199

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  • 5. SNP and haplotype analysis reveals new HFE variants associated with iron overload trait.
    Yang Y, Férec C, Mura C.
    Hum Mutat; 2011 Apr; 32(4):E2104-17. PubMed ID: 21412944
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  • 6. Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.
    Merryweather-Clarke AT, Cadet E, Bomford A, Capron D, Viprakasit V, Miller A, McHugh PJ, Chapman RW, Pointon JJ, Wimhurst VL, Livesey KJ, Tanphaichitr V, Rochette J, Robson KJ.
    Hum Mol Genet; 2003 Sep 01; 12(17):2241-7. PubMed ID: 12915468
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  • 7. Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis.
    Aguilar-Martinez P, Esculié-Coste C, Bismuth M, Giansily-Blaizot M, Larrey D, Schved JF.
    Blood Cells Mol Dis; 2001 Sep 01; 27(1):290-3. PubMed ID: 11358390
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  • 10. Iron overload in HFE C282Y heterozygotes at first genetic testing: a strategy for identifying rare HFE variants.
    Aguilar-Martinez P, Grandchamp B, Cunat S, Cadet E, Blanc F, Nourrit M, Lassoued K, Schved JF, Rochette J.
    Haematologica; 2011 Apr 01; 96(4):507-14. PubMed ID: 21228038
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  • 11. Prevalence of HFE mutations among the Thai population and correlation with iron loading in haemoglobin E disorder.
    Viprakasit V, Vathesathokit P, Chinchang W, Tachavanich K, Pung-Amritt P, Wimhurst VL, Yenchitsomanus PT, Merryweather-Clarke AT, Tanphaichitr VS.
    Eur J Haematol; 2004 Jul 01; 73(1):43-9. PubMed ID: 15182337
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  • 15. Frequency and clinical expression of HFE gene mutations in a Spanish population of subjects with abnormal iron metabolism.
    Gómez-Llorente C, Miranda-León MT, Blanco S, Gandia-Pla S, Gómez-Capilla JA, Fárez-Vidal ME.
    Ann Hematol; 2005 Oct 01; 84(10):650-5. PubMed ID: 15986199
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  • 16. HFE gene mutations in patients with primary iron overload: is there a significant improvement in molecular diagnosis yield with HFE sequencing?
    Santos PC, Pereira AC, Cançado RD, Schettert IT, Sobreira TJ, Oliveira PS, Hirata RD, Hirata MH, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM.
    Blood Cells Mol Dis; 2010 Dec 15; 45(4):302-7. PubMed ID: 20843714
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  • 17. A study of 82 extended HLA haplotypes in HFE-C282Y homozygous hemochromatosis subjects: relationship to the genetic control of CD8+ T-lymphocyte numbers and severity of iron overload.
    Cruz E, Vieira J, Almeida S, Lacerda R, Gartner A, Cardoso CS, Alves H, Porto G.
    BMC Med Genet; 2006 Mar 01; 7():16. PubMed ID: 16509978
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  • 18. Immunohistochemistry of the Hfe protein in patients with hereditary hemochromatosis, iron deficiency anemia, and normal controls.
    Byrnes V, Ryan E, O'Keane C, Crowe J.
    Blood Cells Mol Dis; 2000 Feb 01; 26(1):2-8. PubMed ID: 10772870
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  • 19. Haplotype analysis of the H63D, IVS2+4t/c, and C282Y polymorphisms of the HFE gene reveals rare events of intragenic recombination.
    Curcio M, Fornaciari S, Mariotti ML, Chelazzi S, Scatena F, Presciuttini S.
    Eur J Haematol; 2008 Apr 01; 80(4):341-5. PubMed ID: 18182079
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  • 20. Phenotypic expression of a novel C282Y/R226G compound heterozygous state in HFE hemochromatosis: molecular dynamics and biochemical studies.
    Cézard C, Rabbind Singh A, Le Gac G, Gourlaouen I, Ferec C, Rochette J.
    Blood Cells Mol Dis; 2014 Jan 01; 52(1):27-34. PubMed ID: 23953397
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