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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

69 related articles for article (PubMed ID: 10583922)

  • 1. HFE genotyping using multiplex allele-specific polymerase chain reaction and capillary electrophoresis.
    Lubin IM; Yamada NA; Stansel RM; Pace RG; Rohlfs EM; Silverman LM
    Arch Pathol Lab Med; 1999 Dec; 123(12):1177-81. PubMed ID: 10583922
    [TBL] [Abstract][Full Text] [Related]  

  • 2. High speed single nucleotide polymorphism typing of a hereditary haemochromatosis mutation with capillary array electrophoresis microplates.
    Medintz I; Wong WW; Sensabaugh G; Mathies RA
    Electrophoresis; 2000 Jul; 21(12):2352-8. PubMed ID: 10939445
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Novel method for molecular detection of the two common hereditary hemochromatosis mutations.
    Kaler SG; Devaney JM; Pettit EL; Kirshman R; Marino MA
    Genet Test; 2000; 4(2):125-9. PubMed ID: 10953951
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. A reverse-hybridization assay for the rapid and simultaneous detection of nine HFE gene mutations.
    Oberkanins C; Moritz A; de Villiers JN; Kotze MJ; Kury F
    Genet Test; 2000; 4(2):121-4. PubMed ID: 10953950
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Multiplex analysis of the most common mutations related to hereditary haemochromatosis: two methods combining specific amplification with capillary electrophoresis.
    Gómez-Llorente C; Antúnez A; Blanco S; Suarez A; Gómez-Capilla JA; Farez-Vidal ME
    Eur J Haematol; 2004 Feb; 72(2):121-9. PubMed ID: 14962249
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Genotyping by microdevice electrophoresis.
    Schmalzing D; Koutny L; Adourian A; Chisholm D; Matsudaira P; Ehrlich D
    Methods Mol Biol; 2001; 163():163-73. PubMed ID: 11242941
    [No Abstract]   [Full Text] [Related]  

  • 9. 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]  

  • 10. [The usefulness of the detection of Cys282Tyr and His63Asp mutations in the diagnosis of hereditary hemochromatosis].
    Moreno L; Vallcorba P; Boixeda D; Cabello P; Bermejo F; San Román C
    Rev Clin Esp; 1999 Oct; 199(10):632-6. PubMed ID: 10589245
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Large-scale screening for HFE mutations: methodology and cost.
    Beutler E; Gelbart T
    Genet Test; 2000; 4(2):131-42. PubMed ID: 10953952
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A cheaper and more rapid polymerase chain reaction-restriction fragment length polymorphism method for the detection of the HLA-H gene mutations occurring in hereditary hemochromatosis.
    Lynas C
    Blood; 1997 Nov; 90(10):4235-6. PubMed ID: 9354698
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 14. High-speed DNA genotyping using microfabricated capillary array electrophoresis chips.
    Woolley AT; Sensabaugh GF; Mathies RA
    Anal Chem; 1997 Jun; 69(11):2181-6. PubMed ID: 9183181
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A retrospective anonymous pilot study in screening newborns for HFE mutations in Scandinavian populations.
    Merryweather-Clarke AT; Simonsen H; Shearman JD; Pointon JJ; Nørgaard-Pedersen B; Robson KJ
    Hum Mutat; 1999; 13(2):154-9. PubMed ID: 10094552
    [TBL] [Abstract][Full Text] [Related]  

  • 16. High-performance liquid chromatography multiplex detection of two single nucleotide mutations associated with hereditary hemochromatosis.
    Liang Q; Davis PA; Thompson BH; Simpson JT
    J Chromatogr B Biomed Sci Appl; 2001 Apr; 754(1):265-70. PubMed ID: 11318424
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Alternate splicing produces a soluble form of the hereditary hemochromatosis protein HFE.
    Jeffrey GP; Basclain K; Hajek J; Chakrabarti S; Adams PC
    Blood Cells Mol Dis; 1999 Feb; 25(1):61-7. PubMed ID: 10349514
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases.
    Sham RL; Ou CY; Cappuccio J; Braggins C; Dunnigan K; Phatak PD
    Blood Cells Mol Dis; 1997 Aug; 23(2):314-20. PubMed ID: 9410475
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A high prevalence of HLA-H 845A mutations in hemochromatosis patients and the normal population in eastern England.
    Willis G; Jennings BA; Goodman E; Fellows IW; Wimperis JZ
    Blood Cells Mol Dis; 1997 Aug; 23(2):288-91. PubMed ID: 9410472
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 4.