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Journal Abstract Search

164 related items for PubMed ID: 16849282

  • 1. 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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  • 2. Genetic hemochromatosis, a Celtic disease: is it now time for population screening?
    Byrnes V, Ryan E, Barrett S, Kenny P, Mayne P, Crowe J.
    Genet Test; 2001 Sep; 5(2):127-30. PubMed ID: 11551098
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  • 3. 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 Sep; 8(4):407-10. PubMed ID: 15684872
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  • 4. 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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  • 5. 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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  • 6. Prevalence and penetrance of HFE mutations in 4865 unselected primary care patients.
    Phatak PD, Ryan DH, Cappuccio J, Oakes D, Braggins C, Provenzano K, Eberly S, Sham RL.
    Blood Cells Mol Dis; 2002 Nov 23; 29(1):41-7. PubMed ID: 12482402
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  • 7. 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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  • 8. Frequency of HFE gene mutations C282Y and H63D in Bosnia and Herzegovina.
    Terzić R, Sehić A, Teran N, Terzić I, Peterlin B.
    Coll Antropol; 2006 Sep 23; 30(3):555-7. PubMed ID: 17058523
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  • 12. Prevalence of HFE gene C282Y and H63D mutations in a French-Canadian population of neonates and in referred patients.
    Girouard J, Giguère Y, Delage R, Rousseau F.
    Hum Mol Genet; 2002 Jan 15; 11(2):185-9. PubMed ID: 11809727
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  • 13. Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases?
    Cadet E, Capron D, Gallet M, Omanga-Léké ML, Boutignon H, Julier C, Robson KJ, Rochette J.
    J Med Genet; 2005 May 15; 42(5):390-5. PubMed ID: 15863667
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  • 14. Frequencies of C282Y and H63D mutations and transferrin saturation indices in the Korean population.
    Choi SJ, Min WK, Chun S, Park H, Kim JW, Park CJ, Chi HS.
    Clin Chem Lab Med; 2002 Jul 15; 40(7):689-92. PubMed ID: 12241015
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  • 15. Prevalence of C282Y and H63D mutations in the haemochromatosis (HFE) gene in Tunisian population.
    Sassi R, Hmida S, Kaabi H, Hajjej A, Abid A, Abdelkefi S, Yacoub S, Maamar M, Mojaat N, Ben Hamed L, Bellali H, Dridi A, Jridi A, Midouni B, Boukef MK.
    Ann Genet; 2004 Jul 15; 47(4):325-30. PubMed ID: 15581829
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  • 16. HFE gene and hereditary hemochromatosis: a HuGE review. Human Genome Epidemiology.
    Hanson EH, Imperatore G, Burke W.
    Am J Epidemiol; 2001 Aug 01; 154(3):193-206. PubMed ID: 11479183
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  • 17. Prevalence of H63D, S65C, and C282Y hereditary hemochromatosis gene variants in Madeira Island (Portugal).
    Spínola C, Brehm A, Spínola H.
    Ann Hematol; 2011 Jan 01; 90(1):29-32. PubMed ID: 20714725
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