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Journal Abstract Search

250 related items for PubMed ID: 10545942

  • 1.
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  • 2. 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
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  • 3. 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
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  • 4. Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis.
    Jeffrey GP, Chakrabarti S, Hegele RA, Adams PC.
    Nat Genet; 1999 Aug; 22(4):325-6. PubMed ID: 10431233
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  • 6. [Detection of HFE polymorphism in German patients with hereditary hemochromatosis].
    Burggraf S, Olgemöller B.
    Dtsch Med Wochenschr; 2000 Nov 03; 125(44):1346; author reply 1347. PubMed ID: 11109419
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  • 7. Genotyping as a diagnostic aid in genetic haemochromatosis.
    Rossi E, Henderson S, Chin CY, Olynyk J, Beilby JP, Reed WD, Jeffrey GP.
    J Gastroenterol Hepatol; 1999 May 03; 14(5):427-30. PubMed ID: 10355506
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  • 11. Haemochromatosis: diagnosis and management after the cloning of the HFE gene.
    Powell LW, Bassett ML.
    Aust N Z J Med; 1998 Apr 03; 28(2):159-63. PubMed ID: 9612522
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  • 12. Multicentric origin of hemochromatosis gene (HFE) mutations.
    Rochette J, Pointon JJ, Fisher CA, Perera G, Arambepola M, Arichchi DS, De Silva S, Vandwalle JL, Monti JP, Old JM, Merryweather-Clarke AT, Weatherall DJ, Robson KJ.
    Am J Hum Genet; 1999 Apr 03; 64(4):1056-62. PubMed ID: 10090890
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  • 13. Frequency of the C282Y mutation of hemochromatosis in five French populations.
    Mercier G, Bathelier C, Lucotte G.
    Blood Cells Mol Dis; 1998 Jun 03; 24(2):165-6. PubMed ID: 9642097
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  • 14. What is the role of genetic testing in diagnosis of haemochromatosis?
    Worwood M.
    Ann Clin Biochem; 2001 Jan 03; 38(Pt 1):3-19. PubMed ID: 11270839
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  • 16. Overestimation of HFE C282Y homozygous hemochromatosis prevalence as the result of a common primer-binding site polymorphism.
    Press RD.
    Mol Diagn; 1999 Dec 03; 4(4):391-2. PubMed ID: 10671650
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  • 20. Frequency analysis and allele map in favor of the celtic origin of the C282Y mutation of hemochromatosis.
    Lucotte G.
    Blood Cells Mol Dis; 2001 Dec 03; 27(2):549-56. PubMed ID: 11500066
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