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- 2018
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Mark
Genetic Variation in the Syntaxin-Binding Protein STXBP5 in Type 1 von Willebrand Disease Patients
(
- Contribution to journal › Article
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Mark
Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients
(
- Contribution to journal › Article
- 2011
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Mark
A large deletion identified in a Swedish family with type 1 VWD
(
- Contribution to journal › Letter
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Mark
Variation in the VWF Gene in Swedish Patients with Type 1 von Willebrand Disease.
(
- Contribution to journal › Article
- 2008
-
Mark
Distribution of von Willebrand factor levels in young women with and without bleeding symptoms. Influence of ABO blood group and promoter haplotypes
(
- Contribution to journal › Article
- 2007
-
Mark
Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD)
(
- Contribution to journal › Article
- 2005
-
Mark
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.
(
- Contribution to journal › Article
- 2004
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Mark
Co-segregation of the PROS1 locus and protein S deficiency in families having no detectable mutations in PROS1.
(
- Contribution to journal › Article