Genetic linkage of two intragenic restriction fragment length polymorphisms with von Willebrand's disease type IIA. Evidence for a defect in the von Willebrand factor gene.

Lignende værker

• RFLP for a human von Willebrand factor (vWF) cDNA clone, pvWF1100.
  af: Verweij, C L, et al.
  Udgivet: (1985)
• Severe von Willebrand disease due to a defect at the level of von Willebrand factor mRNA expression: detection by exonic PCR-restriction fragment length polymorphism analysis.
  af: Nichols, W C, et al.
  Udgivet: (1991)
• Restriction fragment length polymorphism linkage map for Arabidopsis thaliana.
  af: Chang, C, et al.
  Udgivet: (1988)
• A polymorphic Xba I site within the human von Willebrand factor (vWF) gene identified by a vWF cDNA clone.
  af: Quadt, R, et al.
  Udgivet: (1986)
• Epitope mapping of the von Willebrand factor subunit distinguishes fragments present in normal and type IIA von Willebrand disease from those generated by plasmin.
  af: Berkowitz, S D, et al.
  Udgivet: (1987)