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Journal Abstract Search

221 related items for PubMed ID: 21736562

  • 1. Simultaneous detection of HFE C282Y, H63D and S65C mutations associated with type 1 haemochromatosis using a multiplex luminex bead assay.
    Cardoso SP, Patel R, Brown C, Navarrete C.
    Tissue Antigens; 2011 Sep; 78(3):171-7. PubMed ID: 21736562
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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. Simultaneous detection of the C282Y, H63D and S65C mutations in the hemochromatosis gene using quenched-FRET real-time PCR.
    Moysés CB, Moreira ES, Asprino PF, Guimarães GS, Alberto FL.
    Braz J Med Biol Res; 2008 Oct 23; 41(10):833-8. PubMed ID: 19030706
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  • 5. 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 Oct 23; 8(3):263-7. PubMed ID: 15727249
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  • 6. 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
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  • 8. 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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  • 9. [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 Apr 23; 151(9):428-31. PubMed ID: 23102134
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  • 10. 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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  • 11. 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 23; 17(10):CR552-6. PubMed ID: 21959608
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  • 14. Linked linear amplification for simultaneous analysis of the two most common hemochromatosis mutations.
    Killeen AA, Breneman JW, Carillo AR, Ugozzoli LA, Lowery JD, Liu J, Hixson CS.
    Clin Chem; 2003 Jul 23; 49(7):1050-7. PubMed ID: 12816900
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  • 15. Frequency of the hemochromatosis gene (HFE) variants in a Jordanian Arab population and in diabetics from the same region.
    Alkhateeb A, Uzrail A, Bodoor K.
    Dis Markers; 2009 Jul 23; 27(1):17-22. PubMed ID: 19822954
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  • 16. Prevalence of the C282Y, H63D, and S65C mutations of the HFE gene in 1,146 newborns from a region of Northern Spain.
    Altes A, Ruiz A, Barceló MJ, Remacha AF, Puig T, Maya AJ, Castell C, Amate JM, Saz Z, Baiget M.
    Genet Test; 2004 Jul 23; 8(4):407-10. PubMed ID: 15684872
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  • 17. 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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  • 18. 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
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  • 19. Genotyping of hemochromatosis-associated mutations in the HFE gene by PCR-RFLP and a novel reverse hybridization method.
    Koeken A, Cobbaert C, Quint W, van Doorn LJ.
    Clin Chem Lab Med; 2002 Feb 23; 40(2):122-5. PubMed ID: 11939483
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  • 20. Analysis of haemochromatosis gene mutations in a population from the Mediterranean Basin.
    Campo S, Restuccia T, Villari D, Raffa G, Cucinotta D, Squadrito G, Pollicino T, Raimondo G.
    Liver; 2001 Aug 23; 21(4):233-6. PubMed ID: 11454185
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