Thrombosis Research
Volume 120 , Pages S11-S16 , 2007

Von Willebrand disease—Phenotype versus genotype: Deficiency versus disease

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  6. Lillicrap D. In: The Basic Science, Diagnosis and Clinical Management of von Willebrand Disease. vol. 35:World Federation of Hemophilia; 2004;
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  13. Eikenboom J, Van Marion V, Putter H, Goodeve A, Rodeghiero F, Castaman G, et al. Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 vWD. J Thromb Haemost. 2006;4:774–782
  14. James PD, Notley C, Hegadorn C, Leggo J, Tuttle A, Tinlin S, et al. The mutational spectrum of type 1 von Willebrand disease: results from a Canadian cohort study. Blood. 2007;109:145–154

PII: S0049-3848(07)00117-X

doi: 10.1016/j.thromres.2007.03.014

Thrombosis Research
Volume 120 , Pages S11-S16 , 2007

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