These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
120 related articles for article (PubMed ID: 11017930)
1. Rapid single-tube screening of the C282Y hemochromatosis mutation by real-time multiplex allele-specific PCR without fluorescent probes. Donohoe GG; Laaksonen M; Pulkki K; Rönnemaa T; Kairisto V Clin Chem; 2000 Oct; 46(10):1540-7. PubMed ID: 11017930 [TBL] [Abstract][Full Text] [Related]
2. Simple multiplex PCR for the simultaneous detection of the C282Y and H63D hemochromatosis (HFE) gene mutations. Stott MK; Fellowes AP; Upton JD; Burt MJ; George PM Clin Chem; 1999 Mar; 45(3):426-8. PubMed ID: 10053052 [No Abstract] [Full Text] [Related]
3. 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]
4. Simultaneous detection of the C282Y, H63D and S65C mutations in the hemochromatosis gene using quenched-FRET real-time PCR. Moysés CB; Moreira ES; Asprino PF; Guimarães GS; Alberto FL Braz J Med Biol Res; 2008 Oct; 41(10):833-8. PubMed ID: 19030706 [TBL] [Abstract][Full Text] [Related]
5. Correction for Stott et al.: simple multiplex PCR for the simultaneous detection of the C282Y and H63D hemochromatosis (HFE) gene mutations. Stott MK; Fellowes AP; Upton JD; Burt MJ; George PM Clin Chem; 2000 Feb; 46(2):308-9. PubMed ID: 10657401 [No Abstract] [Full Text] [Related]
6. Fluorescent multicolor multiplex homogeneous assay for the simultaneous analysis of the two most common hemochromatosis mutations. Ugozzoli LA; Chinn D; Hamby K Anal Biochem; 2002 Aug; 307(1):47-53. PubMed ID: 12137778 [TBL] [Abstract][Full Text] [Related]
7. 5569G/A polymorphism of the HFE gene: no implications for C282Y genotyping in a hemochromatosis screening study of 65,238 individuals. Thorstensen K; Kvitland M; Asberg A; Hveem K Genet Test; 2000; 4(2):147-9. PubMed ID: 10953954 [TBL] [Abstract][Full Text] [Related]
8. 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; 85(8):787-91. PubMed ID: 10942923 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Linked linear amplification for simultaneous analysis of the two most common hemochromatosis mutations. Killeen AA; Breneman JW; Carillo AR; Ugozzoli LA; Lowery JD; Liu J; Hixson CS Clin Chem; 2003 Jul; 49(7):1050-7. PubMed ID: 12816900 [TBL] [Abstract][Full Text] [Related]
11. Genotyping of hemochromatosis-associated mutations in the HFE gene by PCR-RFLP and a novel reverse hybridization method. Koeken A; Cobbaert C; Quint W; van Doorn LJ Clin Chem Lab Med; 2002 Feb; 40(2):122-5. PubMed ID: 11939483 [TBL] [Abstract][Full Text] [Related]
12. Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis. Bittencourt PL; Palácios SA; Couto CA; Cançado EL; Carrilho FJ; Laudanna AA; Kalil J; Gayotto LC; Goldberg AC Braz J Med Biol Res; 2002 Mar; 35(3):329-35. PubMed ID: 11887210 [TBL] [Abstract][Full Text] [Related]
13. An improved real time PCR method for simultaneous detection of C282Y and H63D mutations in the HFE gene associated with hereditary hemochromatosis. Walburger DK; Afonina IA; Wydro R Mutat Res; 2001 Jan; 432(3-4):69-78. PubMed ID: 11465544 [TBL] [Abstract][Full Text] [Related]
15. A novel mutation of HFE explains the classical phenotype of genetic hemochromatosis in a C282Y heterozygote. Wallace DF; Dooley JS; Walker AP Gastroenterology; 1999 Jun; 116(6):1409-12. PubMed ID: 10348824 [TBL] [Abstract][Full Text] [Related]
16. Solid-phase amplification for detection of C282y and H63D hemochromatosis (HFE) gene mutations. Turner MS; Penning S; Sharp A; Hyland VJ; Harris R; Morris CP; van Daal A Clin Chem; 2001 Aug; 47(8):1384-9. PubMed ID: 11468226 [TBL] [Abstract][Full Text] [Related]
17. The role of hemochromatosis susceptibility gene mutations in protecting against iron deficiency in celiac disease. Butterworth JR; Cooper BT; Rosenberg WM; Purkiss M; Jobson S; Hathaway M; Briggs D; Howell WM; Wood GM; Adams DH; Iqbal TH Gastroenterology; 2002 Aug; 123(2):444-9. PubMed ID: 12145797 [TBL] [Abstract][Full Text] [Related]
18. Pitfalls in the genetic diagnosis of hereditary hemochromatosis. Jeffrey GP; Adams PC Genet Test; 2000; 4(2):143-6. PubMed ID: 10953953 [TBL] [Abstract][Full Text] [Related]
19. LightCycler PCR assay for simultaneous detection of the H63D and S65C mutations in the HFE hemochromatosis gene based on opposite melting temperature shifts. Bollhalder M; Mura C; Landt O; Maly FE Clin Chem; 1999 Dec; 45(12):2275-8. PubMed ID: 10585367 [No Abstract] [Full Text] [Related]
20. [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] [Next] [New Search]