The genetics of Canadian type 3 von Willebrand disease: further evidence for co-dominant inheritance of mutant alleles

Common large partialVWFgene deletion does not cause alloantibody formation in the Hungarian type 3 von Willebrand disease population

(2011) A. MOHL et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Large deletions identified in patients with von Willebrand disease using multiple ligation-dependent probe amplification

(2011) H. YADEGARI et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

First application of MLPA method in severe von Willebrand disease. Confirmation of a new large VWF gene deletion and identification of heterozygous carriers

(2010) Noelia Cabrera et al.   BRITISH JOURNAL OF HAEMATOLOGY

A novel deletion mutation is recurrent in von Willebrand disease types 1 and 3

(2009) M. S. Sutherland et al.   BLOOD

Molecular characterization of Iranian patients with type 3 von Willebrand disease

(2009) S. SHAHBAZI et al.   HAEMOPHILIA

Multiplex ligation-dependent probe amplification to detect a large deletion within the von Willebrand gene

(2009) M. ACQUILA et al.   HAEMOPHILIA

The mutation spectrum associated with type 3 von Willebrand disease in a cohort of patients from the North West of England

(2009) M. S. SUTHERLAND et al.   HAEMOPHILIA

The prevalence of symptomatic von Willebrand disease in primary care practice

(2009) M. BOWMAN et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Genetic defects in von Willebrand disease type 3 in Indian and Greek patients

(2008) P.K. Gupta et al.   BLOOD CELLS MOLECULES AND DISEASES

Expression studies of missense mutations p.D141Y, p.C275S located in the propeptide of von Willebrand factor in patients with type 3 von Willebrand disease

(2008) L. BARONCIANI et al.   HAEMOPHILIA

An Alu-mediated novel large deletion is the most frequent cause of type 3 von Willebrand disease in Hungary

(2008) A. MOHL et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Generation and validation of the Condensed MCMDM-1VWD Bleeding Questionnaire for von Willebrand disease

(2008) M. BOWMAN et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS