Multiplex ligation-dependent probe amplification to detect a large deletion within the von Willebrand gene
Author:
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2516.2009.02078.x/fullpdf
Reference5 articles.
1. Von Willebrand factor to the rescue;De Meyer;Blood,2009
2. Clinical and molecular markers of inherited von Willebrand disease type 3: are deletions of the VWF gene associated with alloantibodies to VWF?;Federici;J Thromb Haemost,2008
3. Clearance of von Willebrand factor;Denis;Thromb Haemost,2008
4. Genetic mutations in von Willebrand disease identified by DHPLC and DNA sequence analysis;Kakela;Mol Genet Metab,2006
5. MLPA assay in F8 gene mutation screening;Acquila;Haemophilia,2008
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1. Type 1 von Willebrand Disease in a Pediatric Patient Caused by a Novel Heterozygous Deletion of Exons 1 to 6 of the von Willebrand Factor Gene: A Case Report;Laboratory Medicine;2022-12-05
2. How we make an accurate diagnosis of von Willebrand disease;Thrombosis Research;2020-12
3. Characterization of large in-frame von Willebrand factor deletions highlights differing pathogenic mechanisms;Blood Advances;2020-07-01
4. The molecular basis ofvon Willebrand disease;Molecular Hematology 4e;2019-09-20
5. Von Willebrand disease mutation spectrum and associated mutation mechanisms;Thrombosis Research;2017-11
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