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.


PUBMED FOR HANDHELDS

Journal Abstract Search


128 related items for PubMed ID: 9354698

  • 1. 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 15; 90(10):4235-6. PubMed ID: 9354698
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Hemochromatosis-related mutation detection.
    Merryweather-Clarke AT, Shearman JD, Robson KJ, Pointon JJ, Liu YT, Bomford A, Dooley J, Walker AP, Worwood M.
    Blood; 1998 Apr 01; 91(7):2620-1. PubMed ID: 9516166
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. 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 01; 45(3):426-8. PubMed ID: 10053052
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Frequencies in the Japanese population of HFE gene mutations.
    Sohda T, Yanai J, Soejima H, Tamura K.
    Biochem Genet; 1999 Feb 01; 37(1-2):63-8. PubMed ID: 10429833
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.
    Noll WW, Belloni DR, Stenzel TT, Grody WW.
    Nat Genet; 1999 Nov 01; 23(3):271-2. PubMed ID: 10610176
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Incorrect diagnosis of hereditary hemochromatosis.
    Mirochnik O, Halim-Kertanegara N, Hertzberg M, McDonald D, Liddle C.
    Am J Hematol; 2000 Feb 01; 63(2):104-5. PubMed ID: 10629581
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Simple and rapid detection of the newly described mutations in the HLA-H gene.
    Aguilar Martinez P, Jeanjean P, Masmejean C, Guillard A, Biron C, Rabesandratana H, Schved JF.
    Blood; 1997 Mar 01; 89(5):1835-6. PubMed ID: 9057671
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Denaturing gradient gel electrophoresis analysis of the hemochromatosis (HFE) gene: impact of HFE gene mutations on the manifestation of porphyria cutanea tarda.
    Christiansen L, Bygum A, Thomsen K, Brandrup F, Hørder M, Petersen NE.
    Clin Chem; 1999 Nov 01; 45(11):2025-6. PubMed ID: 10545080
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 7.