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Journal Abstract Search

138 related items for PubMed ID: 9232622

  • 1. 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
    [No Abstract] [Full Text] [Related]

  • 2. Two novel polymorphisms (E277K and V212V) in the haemochromatosis gene HFE.
    Bradbury R, Fagan E, Payne SJ.
    Hum Mutat; 2000 Jan; 15(1):120. PubMed ID: 10612845
    [No Abstract] [Full Text] [Related]

  • 3. 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
    [No Abstract] [Full Text] [Related]

  • 4. Detection of C282Y and H63D in the HFE gene.
    Pointon JJ, Merryweather-Clarke AT, Carella M, Robson KJ.
    Genet Test; 2000 Feb; 4(2):115-20. PubMed ID: 10953949
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  • 5. Rapid diagnosis of hemochromatosis gene Cys282Tyr mutation by SSCP analysis.
    Hertzberg MS, McDonald D, Mirochnik O.
    Am J Hematol; 1998 Mar; 57(3):260-1. PubMed ID: 9495384
    [No Abstract] [Full Text] [Related]

  • 6. 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]

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  • 18. [Molecular genetic diagnosis in hemochromatosis].
    Gehrke SG, Stremmel W.
    Dtsch Med Wochenschr; 1999 Apr 09; 124(14):431-4. PubMed ID: 10230385
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  • 19. Frequencies in the Japanese population of HFE gene mutations.
    Sohda T, Yanai J, Soejima H, Tamura K.
    Biochem Genet; 1999 Feb 09; 37(1-2):63-8. PubMed ID: 10429833
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  • 20. Genetic hemochromatosis: why is discovery of the HLA-H gene of interest to rheumatologists?
    Puéchal X.
    Rev Rhum Engl Ed; 1997 Oct 09; 64(10):527-9. PubMed ID: 9385688
    [No Abstract] [Full Text] [Related]

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