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Journal Abstract Search

215 related items for PubMed ID: 9569179

  • 21. [Molecular study of type 2 von Willebrand disease].
    Habart D, Smejkal P, Matýsková M, Turek P, Hrachovinová I, Vorlová Z.
    Cas Lek Cesk; 2003; 142(6):373-6. PubMed ID: 12924038
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  • 22. Recessive von Willebrand disease type 2 Normandy: variable expression of mild hemophilia and VWD type 1.
    Michiels JJ, Gadisseur A, Vangenegten I, Schroyens W, Berneman Z.
    Acta Haematol; 2009; 121(2-3):119-27. PubMed ID: 19506358
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  • 23. A common splice site mutation is shared by two families with different type 2N von Willebrand disease mutations.
    Nesbitt IM, Hampton KK, Preston FE, Peake IR, Goodeve AC.
    Thromb Haemost; 1999 Sep; 82(3):1061-4. PubMed ID: 10494764
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  • 25. Mutations in von Willebrand factor multimerization domains are not a common cause of classical type 1 von Willebrand disease.
    Keeney S, Cumming A, Hay C.
    Thromb Haemost; 1999 Nov; 82(5):1446-50. PubMed ID: 10595636
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  • 27. A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation.
    Shen MC, Lin JS, Lin DS, Hsu SC, Lin B.
    Thromb Res; 2003 Nov; 112(5-6):291-5. PubMed ID: 15041272
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  • 29. Impaired dimerization of von Willebrand factor subunit due to mutation A2801D in the CK domain results in a recessive type 2A subtype IID von Willebrand disease.
    Hommais A, Stépanian A, Fressinaud E, Mazurier C, Pouymayou K, Meyer D, Girma JP, Ribba AS.
    Thromb Haemost; 2006 May; 95(5):776-81. PubMed ID: 16676067
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  • 30. Autosomal recessive von Willebrand disease type 1 or 2 due to homozygous or compound heterozygous mutations in the von Willebrand factor gene. A single center experience on molecular heterogeneity and laboratory features in 12 families.
    Castaman G, Giacomelli S, Rodeghiero F.
    Acta Haematol; 2009 May; 121(2-3):106-10. PubMed ID: 19506356
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  • 32. Characterization of von Willebrand factor gene defects in two unrelated patients with type IIC von Willebrand disease.
    Gaucher C, Diéval J, Mazurier C.
    Blood; 1994 Aug 15; 84(4):1024-30. PubMed ID: 8049421
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  • 35. Von Willebrand's disease: a novel mutation, P1824H and the incidence of R1205H defect among families with dominant quantitative von Willebrand factor deficiency.
    Casaña P, Cabrera N, Haya S, Cid AR, Aznar JA.
    Haematologica; 2006 Aug 15; 91(8):1130-3. PubMed ID: 16870550
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