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25. [Genetic hemochromatosis and the HFE gene: from molecular genetics to clinical diagnosis]. Höhler T; Gerken G Z Gastroenterol; 2000 Jun; 38(6):509-15. PubMed ID: 10923364 [TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. [Frequency of HFE gene mutations and genotype-phenotype correlations in patients with hereditary hemochromatosis in Switzerland]. Himmelmann A; Bortoluzzi L; Jansen S; Fehr J Schweiz Med Wochenschr; 2000 Aug; 130(31-32):1112-9. PubMed ID: 11008304 [TBL] [Abstract][Full Text] [Related]
30. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. Gomez PS; Parks S; Ries R; Tran TC; Gomez PF; Press RD Nat Genet; 1999 Nov; 23(3):272. PubMed ID: 10545944 [No Abstract] [Full Text] [Related]
31. Mutation analysis of the HFE gene associated with hereditary hemochromatosis in a Venezuelan sample. Vizzi E; Loureiro CL; Gerder M; de las Nieves Garcia-Casal M; Rodríguez-Larralde A; Gerace L; Ludert JE; Liprandi F; Pujol FH Ann Hematol; 2005 Nov; 84(12):802-6. PubMed ID: 15995871 [TBL] [Abstract][Full Text] [Related]
32. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results. Noll WW; Belloni DR; Stenzel TT; Grody WW Nat Genet; 1999 Nov; 23(3):271-2. PubMed ID: 10610176 [No Abstract] [Full Text] [Related]
33. Genetic hemochromatosis update. Brissot P; Le Lan C; Lorho R; Gaboriau F; Lescoat G; Loréal O Acta Gastroenterol Belg; 2005; 68(1):33-7. PubMed ID: 15832585 [TBL] [Abstract][Full Text] [Related]
34. 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]
35. Use of denaturing HPLC and a heteroduplex generator to detect the HFE C282Y mutation associated with genetic hemochromatosis. Fruchon S; Bensaid M; Borot N; Roth MP; Coppin H Clin Chem; 2003 May; 49(5):822-4. PubMed ID: 12709380 [No Abstract] [Full Text] [Related]
36. HFE gene mutations are extremely rare in Western sub-Saharan Africa. Martins R; Picanço I; Nunes B; Romão L; Faustino P Ann Hematol; 2005 Oct; 84(10):686-8. PubMed ID: 15834568 [No Abstract] [Full Text] [Related]
37. Definition of C282Y mutation in a hereditary hemochromatosis family from Turkey. Yönal O; Hatirnaz O; Akyüz F; Köroğlu G; Ozbek U; Cefle K; Mungan Z Turk J Gastroenterol; 2007 Mar; 18(1):53-7. PubMed ID: 17450498 [TBL] [Abstract][Full Text] [Related]
38. HFE genotype frequencies in consecutive reference laboratory specimens: comparisons among referral sources and association with initial diagnosis. Acton RT; Barton JC Genet Test; 2001; 5(4):299-306. PubMed ID: 11960574 [TBL] [Abstract][Full Text] [Related]
39. Uncommon mutations and polymorphisms in the hemochromatosis gene. Pointon JJ; Wallace D; Merryweather-Clarke AT; Robson KJ Genet Test; 2000; 4(2):151-61. PubMed ID: 10953955 [TBL] [Abstract][Full Text] [Related]
40. Impact of HFE genetic testing on clinical presentation of hereditary hemochromatosis: new epidemiological data. Scotet V; Le Gac G; Mérour MC; Mercier AY; Chanu B; Ka C; Mura C; Nousbaum JB; Férec C BMC Med Genet; 2005 Jun; 6():24. PubMed ID: 15929798 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]