Two Populations of Factor VIII-Related Antigen in a Family with von Willebrand's Disease
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1979.tb05856.x/fullpdf
Reference15 articles.
1. Assay of Ristocetin Co-factor using Fixed Platelets and a Platelet Counting Technique
2. Von Willebrand’s Disease
3. Genetic Variants of von Willebrand's Disease
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1. A new candidate mutation (N528S) within the von Willebrand factor propeptide identified in a Japanese patient with phenotype IIC of von Willebrand disease;European Journal of Haematology;2009-04-24
2. Laboratory and Molecular Characteristics of Recessive von Willebrand Disease Type 2C (2A Subtype IIC) of Variable Severity due to Homozygous or Double Heterozygous Mutations in the D1 and D2 Domains;Acta Haematologica;2009
3. Von Willebrand factor multimer patterns in von Willebrand's disease;British Journal of Haematology;2008-07-07
4. The varieties of von Willebrand's disease;Clinical & Laboratory Haematology;2008-06-28
5. Characterization of Recessive Severe Type 1 and 3 von Willebrand Disease (VWD), Asymptomatic Heterozygous Carriers Versus Bloodgroup O-Related von Willebrand Factor Deficiency, and Dominant Type 1 VWD;Clinical and Applied Thrombosis/Hemostasis;2006-07
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