Genetic analysis of 31 Swedish type 1 von Willebrand disease families reveals incomplete linkage to the von Willebrand factor gene and a high frequency of a certain disease haplotype
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2005.01631.x/fullpdf
Reference29 articles.
1. A Revised Classification of von Willebrand Disease
2. Genetics of classic von Willebrand's disease. I. Phenotypic variation within families
3. Structure of the gene for human von Willebrand factor
4. Human von Willebrand factor gene and pseudogene: structural analysis and differentiation by polymerase chain reaction
5. Congenital von Willebrand disease type 1: definition, phenotypes, clinical and laboratory assessment
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2. Von Willebrand factor levels in healthy blood donors and their association with blood group;Asian Journal of Transfusion Science;2023-01
3. Prevalence of von Willebrand Disease in Patients with Heavy Menstrual Bleeding: An Indian Perspective;Journal of South Asian Federation of Obstetrics and Gynaecology;2022-03-04
4. Common and Rare Variants in Genes Associated with von Willebrand Factor Level Variation: No Accumulation of Rare Variants in Swedish von Willebrand Disease Patients;TH Open;2020-10
5. Targeted re-sequencing of F8, F9 and VWF: Characterization of Ion Torrent data and clinical implications for mutation screening;PLOS ONE;2019-04-26
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