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8. Mutations of the HFE gene among Turkish hereditary hemochromatosis patients. Simsek H; Balaban YH; Yilmaz E; Sumer H; Buyukasik Y; Cengiz C; Ozcebe O; Hascelik G; Tatar G Ann Hematol; 2005 Oct; 84(10):646-9. PubMed ID: 15871018 [TBL] [Abstract][Full Text] [Related]
9. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. The European Haemochromatosis Consortium. Merryweather-Clarke AT; Pointon JJ; Shearman JD; Robson KJ; Jouanolle AM; Mosser A; David V; Le Gall JY; Halsall DJ; Elsey TS; Kelly A; Cox TM; Clare M; Bomford A; Vandwalle JL; Rochette J; Borot N; Coppin H; Roth MP; Ryan E; Crowe J; Totaro A; Gasparini P; Roetto A; Walker AP Nat Genet; 1999 Nov; 23(3):271. PubMed ID: 10545942 [No Abstract] [Full Text] [Related]
10. The HFE Cys282Tyr mutation as a necessary but not sufficient cause of clinical hereditary hemochromatosis. Beutler E Blood; 2003 May; 101(9):3347-50. PubMed ID: 12707220 [No Abstract] [Full Text] [Related]
11. No age-related decrease in frequency of heterozygotes for the HFE C282Y haemochromatosis mutation. Waalen J; Beutler E J Hepatol; 2004 Jun; 40(6):1044; author reply 1044-5. PubMed ID: 15158353 [No Abstract] [Full Text] [Related]
12. The geography of HFE mutations: molecular diagnosis of haemochromatosis and the globalization of genetic testing. Salto-Tellez M; Siew-Chuan Koay E Eur J Hum Genet; 2004 Nov; 12(11):877-8. PubMed ID: 15340365 [No Abstract] [Full Text] [Related]
19. Characterization of the second HFE gross deletion highlights the potential importance of Alu-mediated recombination in haemochromatosis. Ka C; Chen JM; Gourlaouen I; Quemener S; Ronsin C; Massonnet S; Thérond JP; Férec C; Le Gac G Br J Haematol; 2015 Mar; 168(5):759-62. PubMed ID: 25284364 [No Abstract] [Full Text] [Related]
20. Frequency of the C282Y mutation of hemochromatosis in five French populations. Mercier G; Bathelier C; Lucotte G Blood Cells Mol Dis; 1998 Jun; 24(2):165-6. PubMed ID: 9642097 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]