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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

145 related items for PubMed ID: 9495384

  • 1.
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  • 2. Incorrect diagnosis of hereditary hemochromatosis.
    Mirochnik O, Halim-Kertanegara N, Hertzberg M, McDonald D, Liddle C.
    Am J Hematol; 2000 Feb; 63(2):104-5. PubMed ID: 10629581
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  • 3. [Genetic background and DNA diagnostics of hemochromatosis].
    Heliö T, Färkkilä M, Halme L, Karlsson M, Palotie A, Kontula K.
    Duodecim; 1998 Feb; 114(14):1404-9. PubMed ID: 11552248
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  • 4. Hereditary hemochromatosis: a HpaI polymorphism within the HLA-H gene.
    Totaro A, Grifa A, Carella M, D'Ambrosio L, Valentino M, Roth MP, Borot N, Coppin H, Roetto A, Camaschella C, Gasparini P.
    Mol Cell Probes; 1997 Jun; 11(3):229-30. PubMed ID: 9232622
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  • 6. Rapid diagnosis of the HLA-H gene Cys 282 Tyr mutation in hemochromatosis by polymerase chain reaction--a very rare mutation in the Chinese population.
    Chang JG, Liu TC, Lin SF.
    Blood; 1997 May 01; 89(9):3492-3. PubMed ID: 9129062
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  • 8. Detection of C282Y and H63D in the HFE gene.
    Pointon JJ, Merryweather-Clarke AT, Carella M, Robson KJ.
    Genet Test; 2000 May 01; 4(2):115-20. PubMed ID: 10953949
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  • 10. [Clinical usefulness of the detection of mutations of the HFE gene in hemochromatosis].
    Oliva R, Sánchez M, Bruguera M, Rodés J.
    Gastroenterol Hepatol; 2000 Nov 01; 23(9):433-5. PubMed ID: 11126040
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  • 12. [Detection of HFE polymorphism in German patients with hereditary hemochromatosis].
    Mensing HJ.
    Dtsch Med Wochenschr; 2000 Nov 03; 125(44):1346-7. PubMed ID: 11109420
    [No Abstract] [Full Text] [Related]

  • 13. Haemochromatosis: automated detection of the two point mutations in the HFE gene: Cys282Tyr and His63Asp.
    Klingler KR, Zech D, Wielckens K.
    Clin Chem Lab Med; 2000 Dec 03; 38(12):1225-30. PubMed ID: 11205685
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  • 18. Rapid genotyping of hemochromatosis gene mutations on the LightCycler with fluorescent hybridization probes.
    Mangasser-Stephan K, Tag C, Reiser A, Gressner AM.
    Clin Chem; 1999 Oct 03; 45(10):1875-8. PubMed ID: 10508142
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