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Journal Abstract Search


99 related items for PubMed ID: 12651261

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  • 26. Hereditary hemochromatosis: detection of C282Y and H63D mutations in HFE gene by means of guthrie cards in population of Czech Republic.
    Cimburova M, Putova I, Provaznikova H, Horak J.
    Genet Epidemiol; 2002 Oct; 23(3):260-3. PubMed ID: 12384978
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  • 30. Prevalence of HFE mutations in California newborns.
    Hoppe C, Watson RM, Long CM, Lorey F, Robles L, Klitz W, Styles L, Vichinsky E.
    Pediatr Hematol Oncol; 2006 Sep; 23(6):507-16. PubMed ID: 16849282
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  • 31. Linkage disequilibrium between S65C HFE mutation and HLA A29-B44 haplotype in Terceira Island, Azores.
    Couto AR, Peixoto MJ, Garrett F, Laranjeira F, Cipriano T, Armas JB.
    Hum Immunol; 2003 Jun; 64(6):625-8. PubMed ID: 12770794
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  • 32. Frequencies of the haemochromatosis gene (HFE) variants C282Y, H63D and S65C in 6,020 ethnic Danish men.
    Pedersen P, Melsen GV, Milman N.
    Ann Hematol; 2008 Sep; 87(9):735-40. PubMed ID: 18542962
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  • 37. Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000).
    Martinelli AL, Filho R, Cruz S, Franco R, Tavella M, Secaf M, Ramalho L, Zucoloto S, Rodrigues S, Zago M.
    Genet Mol Res; 2005 Mar 31; 4(1):31-8. PubMed ID: 15841433
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  • 38. Abnormal regulation of HFE mRNA expression does not contribute to primary iron overload.
    Vercesi E, Cerani P, Rolandi V, Rovati A, Bergamaschi G.
    Haematologica; 2000 Aug 31; 85(8):787-91. PubMed ID: 10942923
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