An infrequent DNA polymorphism associated with severe von Willebrand's disease
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1990.tb02619.x/fullpdf
Reference31 articles.
1. Carrier Detection in Severe (Type III) von Willebrand Disease Using Two Intragenic Restriction Fragment Length Polymorphisms
2. Von Willebrand disease investigated by two novel RFLPs
3. Bleeding time, blood groups and von Willebrand factor
4. The effect of ABO blood group on the diagnosis of von Willebrand disease
5. Human von Willebrand Factor (vWF): Isolation of Complementary DNA (cDNA) Clones and Chromosomal Localization
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1. The molecular biology of von Willebrand disease;Clinical & Laboratory Haematology;2001-08-01
2. Congenital von Willebrand disease type 3: clinical manifestations, pathophysiology and molecular biology;Best Practice & Research Clinical Haematology;2001-06
3. von Willebrand Disease;Medicine;1997-01
4. von Willebrand disease: Pathogenesis, classification, and management;Transfusion Medicine Reviews;1996-04
5. The inheritance and molecular genetics of von Willebrand's disease;Haemophilia;1995-04
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