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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

109 related items for PubMed ID: 7546452

  • 41.
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  • 42. Prevalence of small rearrangements in the factor VIII gene F8C among patients with severe hemophilia A.
    Bogdanova N, Markoff A, Pollmann H, Nowak-Göttl U, Eisert R, Dworniczak B, Eigel A, Horst J.
    Hum Mutat; 2002 Sep; 20(3):236-7. PubMed ID: 12204009
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  • 43.
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  • 45. Carrier detection and prenatal diagnosis of hemophilia Alpha.
    Liu Y, Wang X, Chu H, Li Z, Wang H, Wang Z.
    Chin Med J (Engl); 2002 Jul; 115(7):991-4. PubMed ID: 12150727
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  • 46. Utility of a (GT) dinucleotide repeat in intron 1 of the factor 8 gene for haemophilia A carrier diagnosis.
    Tizzano E, Venceslá A, Cornet M, Baena M, Baiget M.
    Haemophilia; 2005 Mar; 11(2):142-4. PubMed ID: 15810916
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  • 47. Carrier detection by DNA linkage analysis in eighty Thai hemophilia A families.
    Mahasandana C, Pung-Amritt P, Treesucon A, Petrarat S, Veerakul G, Visudhiphan S, Yenchitsomanus PT.
    J Med Assoc Thai; 2002 Aug; 85 Suppl 2():S513-21. PubMed ID: 12403227
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  • 48. Direct detection of a missense mutation causing severe hemophilia A by PCR amplification and fluorescence scanning.
    Marchetti G, Gemmati D, Patracchini P, Volinia S, Castagnoli A, Tosi B, Capelli M, Bernardi F.
    Hematol Pathol; 1990 Aug; 4(4):185-8. PubMed ID: 2074260
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  • 49.
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  • 52.
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  • 53. Haemophilia management in New Zealand: an Auckland perspective.
    Ockelford PA, Benny AG, Van de Water NS, Berry EW.
    N Z Med J; 1989 Apr 26; 102(866):189-91. PubMed ID: 2496366
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  • 54. Analysis of factor VIII gene inversion mutations in 166 unrelated haemophilia A families: frequency and utility in genetic counselling.
    Vnencak-Jones CL, Phillips J, Janco RL, Cohen MP, Dupont WD, Kazazian HH, Rossiter JP.
    Haemophilia; 1996 Jan 26; 2(1):18-23. PubMed ID: 27213900
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  • 55. [Hemophilia, carrier state and prenatal diagnosis].
    Sixma JJ.
    Ned Tijdschr Geneeskd; 1984 Feb 25; 128(8):360-2. PubMed ID: 6700781
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  • 56. [Detection of carrier state of hemophilia; current status].
    Briët E, Bröcker-Vriends A, Hermans J.
    Ned Tijdschr Geneeskd; 1984 Feb 25; 128(8):354-60. PubMed ID: 6700780
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  • 57. [Carrier diagnosis as a principle of genetic counseling in hemophilia A].
    Plendl H, Grote W.
    Med Welt; 1982 Oct 22; 33(42):1483-4. PubMed ID: 7176873
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  • 58. [Detection of hemophilia carrier and prenatal diagnosis].
    Kazama M.
    Nihon Rinsho; 1981 Oct 22; 39(12):3737-41. PubMed ID: 7040731
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  • 59.
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  • 60.
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