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Journal Abstract Search

332 related items for PubMed ID: 21959608

  • 1. Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosis.
    Milić S, Ristić S, Starčević-Čizmarević N, Brajenović-Milić B, Crnić-Martinović M, Kapović M, Peterlin B, Štimac D.
    Med Sci Monit; 2011 Oct; 17(10):CR552-6. PubMed ID: 21959608
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  • 2. Prevalence of H63D, S65C and C282Y hereditary hemochromatosis gene mutations in Slovenian population by an improved high-throughput genotyping assay.
    Cukjati M, Vaupotic T, Rupreht R, Curin-Serbec V.
    BMC Med Genet; 2007 Nov 23; 8():69. PubMed ID: 18036208
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  • 3. Frequency of HFE H63D, S65C, and C282Y mutations in patients with iron overload and controls from Toledo, Spain.
    de Diego C, Murga MJ, Martínez-Castro P.
    Genet Test; 2004 Nov 23; 8(3):263-7. PubMed ID: 15727249
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  • 4. HFE gene C282Y, H63D and S65C mutations frequency in the Transylvania region, Romania.
    Trifa AP, Popp RA, Militaru MS, Farcaş MF, Crişan TO, Gana I, Cucuianu A, Pop IV.
    J Gastrointestin Liver Dis; 2012 Jun 23; 21(2):177-80. PubMed ID: 22720307
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  • 5. Prevalence of C282Y, H63D, and S65C mutations in hereditary HFE-hemochromatosis gene in Lithuanian population.
    Kucinskas L, Juzenas S, Sventoraityte J, Cedaviciute R, Vitkauskiene A, Kalibatas V, Kondrackiene J, Kupcinskas L.
    Ann Hematol; 2012 Apr 23; 91(4):491-5. PubMed ID: 21947086
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  • 6. HFE mutations and hemochromatosis in Danish patients admitted for HFE genotyping.
    Koefoed P, Dalhoff K, Dissing J, Kramer I, Milman N, Pedersen P, Simonsen K, Tygstrup N, Nielsen FC.
    Scand J Clin Lab Invest; 2002 Apr 23; 62(7):527-35. PubMed ID: 12512743
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  • 7. Frequency of the hemochromatosis HFE mutations C282Y, H63D, and S65C in blood donors in the Faroe Islands.
    Milman N, á Steig T, Koefoed P, Pedersen P, Fenger K, Nielsen FC.
    Ann Hematol; 2005 Mar 23; 84(3):146-9. PubMed ID: 15042317
    [Abstract] [Full Text] [Related]

  • 8. Analysis of the HFE gene (C282Y, H63D and S65C) mutations in a general Chinese Han population.
    Lin A, Yan WH, Xu HH, Zhu M, Zhou MY.
    Tissue Antigens; 2007 Sep 23; 70(3):252-5. PubMed ID: 17661915
    [Abstract] [Full Text] [Related]

  • 9. Analysis of HFE gene mutations (C282Y, H63D, and S65C) in the Ecuadorian population.
    Leone PE, Giménez P, Collantes JC, Paz-y-Miño C.
    Ann Hematol; 2005 Feb 23; 84(2):103-5. PubMed ID: 15517265
    [Abstract] [Full Text] [Related]

  • 10. Mutation analysis of the HFE gene in German hemochromatosis patients and controls using automated SSCP-based capillary electrophoresis and a new PCR-ELISA technique.
    Hellerbrand C, Bosserhoff AK, Seegers S, Lingner G, Wrede C, Lock G, Schölmerich J, Büttner R.
    Scand J Gastroenterol; 2001 Nov 23; 36(11):1211-6. PubMed ID: 11686223
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  • 12. [The importance of DNA analysis of C282Y, H63D and S65C mutations in the HFE gene].
    Drastíková M, Beránek M, Hegerová J, Putzová D.
    Cas Lek Cesk; 2012 Nov 23; 151(9):428-31. PubMed ID: 23102134
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  • 16. S65C and other mutations in the haemochromatosis gene in the Czech population.
    Cimburová M, Půtová I, Provazníková H, Pintérová D, Horák J.
    Folia Biol (Praha); 2005 Nov 23; 51(6):172-6. PubMed ID: 16419611
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  • 20. Analysis of HFE genes C282Y, H63D, and S65D in patients with hyperferritinemia from northeastern Brazil.
    Leão GD, Freire JM, Cunha Fernandes AL, Moura de Oliveira TM, Leão ND, Gil EA, de Vasconcelos RC, Azevedo JP, de Farias Sales VS, de Araújo Moura Lemos TM, Leão MD, do Nascimento FF, Maciel JF, de Freitas RV, de Souza Paiva A, Cavalcanti GB.
    J Clin Lab Anal; 2014 May 23; 28(3):178-85. PubMed ID: 24395214
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