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Journal Abstract Search

111 related items for PubMed ID: 28696025

  • 1. A novel VWF variant associated with type 2 von Willebrand disease in German Wirehaired Pointers and German Shorthaired Pointers.
    Vos-Loohuis M, van Oost BA, Dangel C, Langbein-Detsch I, Leegwater PA.
    Anim Genet; 2017 Aug; 48(4):493-496. PubMed ID: 28696025
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  • 2. A von Willebrand's factor genomic nucleotide variant and polymerase chain reaction diagnostic test associated with inheritable type-2 von Willebrand's disease in a line of german shorthaired pointer dogs.
    Kramer JW, Venta PJ, Klein SR, Cao Y, Schall WD, Yuzbasiyan-Gurkan V.
    Vet Pathol; 2004 May; 41(3):221-8. PubMed ID: 15133170
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  • 5. Estimated prevalence of canine Type 2 Von Willebrand disease in the Deutsch-Drahthaar (German Wirehaired Pointer) in Europe.
    Gavazza A, Presciuttini S, Keuper H, Lubas G.
    Res Vet Sci; 2012 Dec; 93(3):1462-6. PubMed ID: 22824509
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  • 13. Laboratory diagnosis and molecular classification of von Willebrand disease.
    Gadisseur A, Hermans C, Berneman Z, Schroyens W, Deckmyn H, Michiels JJ.
    Acta Haematol; 2009 Dec; 121(2-3):71-84. PubMed ID: 19506352
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  • 18. The genetic defect of type I von Willebrand disease "Vicenza" is linked to the von Willebrand factor gene.
    Randi AM, Sacchi E, Castaman GC, Rodeghiero F, Mannucci PM.
    Thromb Haemost; 1993 Feb 01; 69(2):173-6. PubMed ID: 8456430
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  • 19. Nonsense mediated decay of VWF mRNA subsequent to c.7674-7675insC mutation in type3 VWD patients.
    Shahbazi S, Baniahmad F, Zakiani-Roudsari M, Raigani M, Mahdian R.
    Blood Cells Mol Dis; 2012 Jun 15; 49(1):48-52. PubMed ID: 22503077
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  • 20. 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 15; 82(5):1446-50. PubMed ID: 10595636
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