473 related articles for article (PubMed ID: 15517265)
1. 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; 84(2):103-5. PubMed ID: 15517265
[TBL] [Abstract][Full Text] [Related]
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; 8():69. PubMed ID: 18036208
[TBL] [Abstract][Full Text] [Related]
3. [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; 151(9):428-31. PubMed ID: 23102134
[TBL] [Abstract][Full Text] [Related]
4. 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; 91(4):491-5. PubMed ID: 21947086
[TBL] [Abstract][Full Text] [Related]
5. HFE gene C282Y, H63D and S65C mutations frequency in the Transylvania region, Romania.
Trifa AP; Popp RA; Militaru MS; Farcaş MF; Crişan TO; Gana I; Cucuianu A; Pop IV
J Gastrointestin Liver Dis; 2012 Jun; 21(2):177-80. PubMed ID: 22720307
[TBL] [Abstract][Full Text] [Related]
6. Frequency of the hemochromatosis HFE mutations C282Y, H63D, and S65C in blood donors in the Faroe Islands.
Milman N; á Steig T; Koefoed P; Pedersen P; Fenger K; Nielsen FC
Ann Hematol; 2005 Mar; 84(3):146-9. PubMed ID: 15042317
[TBL] [Abstract][Full Text] [Related]
7. Prevalence of H63D, S65C, and C282Y hereditary hemochromatosis gene variants in Madeira Island (Portugal).
Spínola C; Brehm A; Spínola H
Ann Hematol; 2011 Jan; 90(1):29-32. PubMed ID: 20714725
[TBL] [Abstract][Full Text] [Related]
8. 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; 70(3):252-5. PubMed ID: 17661915
[TBL] [Abstract][Full Text] [Related]
9. 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; 8(4):407-10. PubMed ID: 15684872
[TBL] [Abstract][Full Text] [Related]
10. 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; 8(3):263-7. PubMed ID: 15727249
[TBL] [Abstract][Full Text] [Related]
11. S65C and other mutations in the haemochromatosis gene in the Czech population.
Cimburová M; Půtová I; Provazníková H; Pintérová D; Horák J
Folia Biol (Praha); 2005; 51(6):172-6. PubMed ID: 16419611
[TBL] [Abstract][Full Text] [Related]
12. 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; 17(10):CR552-6. PubMed ID: 21959608
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands.
Barton JC; Sawada-Hirai R; Rothenberg BE; Acton RT
Blood Cells Mol Dis; 1999; 25(3-4):147-55. PubMed ID: 10575540
[TBL] [Abstract][Full Text] [Related]
15. HFE gene mutations an Apulian population: allele frequencies.
Pietrapertosa A; Vitucci A; Campanale D; Palma A; Renni R; Delios G; Tannoia N
Eur J Epidemiol; 2003; 18(7):685-9. PubMed ID: 12952143
[TBL] [Abstract][Full Text] [Related]
16. 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
[TBL] [Abstract][Full Text] [Related]
17. 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; 27(1):17-22. PubMed ID: 19822954
[TBL] [Abstract][Full Text] [Related]
18. Hereditary hemochromatosis gene (HFE) mutations C282Y, H63D and S65C in patients with idiopathic dilated cardiomyopathy.
Hannuksela J; Leppilampi M; Peuhkurinen K; Kärkkäinen S; Saastamoinen E; Heliö T; Kaartinen M; Nieminen MS; Nieminen P; Parkkila S
Eur J Heart Fail; 2005 Jan; 7(1):103-8. PubMed ID: 15642540
[TBL] [Abstract][Full Text] [Related]
19. 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; 47(4):325-30. PubMed ID: 15581829
[TBL] [Abstract][Full Text] [Related]
20. 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
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]