An association of candidate gene haplotypes and bleeding severity in von Willebrand disease type 2A, 2B, and 2M pedigrees

Journal of Thrombosis and Haemostasis

Volumn 4, Issue 1, 2006, Pages 137-147

  Kunicki, Tom J ^a   Baronciani, L ^b   Canciani, M T ^b   Gianniello, F ^b   Head, S R ^a   Mondala, T S ^a   Salomon, D R ^a   Federici, A B ^a  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

^b UNIVERSITY OF MILAN   (Italy)

Author keywords

Bleeding; Gene; ITGA2; Risk; Von Willebrand disease

Indexed keywords

ALPHA2 INTEGRIN; ANTIGEN; COLLAGEN RECEPTOR; RISTOCETIN; VON WILLEBRAND FACTOR;

ARTICLE; BLEEDING; CONTROLLED STUDY; CORRELATION ANALYSIS; DISEASE CLASSIFICATION; DISEASE SEVERITY; DNA POLYMORPHISM; GENE MUTATION; GENETIC ASSOCIATION; GENOTYPE; HAPLOTYPE; HEMOSTASIS; HUMAN; MAJOR CLINICAL STUDY; MORBIDITY; PEDIGREE; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN EXPRESSION; RISK FACTOR; STATISTICAL SIGNIFICANCE; THROMBOCYTE; VON WILLEBRAND DISEASE; ADOLESCENT; ADULT; AGED; BIOLOGICAL MODEL; BLOOD; CHILD; FEMALE; GENETICS; HOSPITALIZATION; MALE; MIDDLE AGED; MUTATION; PROMOTER REGION;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; CHILD; FEMALE; GENOTYPE; HAPLOTYPES; HEMORRHAGE; HUMANS; INTEGRIN ALPHA2; MALE; MIDDLE AGED; MODELS, GENETIC; MUTATION; PEDIGREE; PROMOTER REGIONS (GENETICS); SEVERITY OF ILLNESS INDEX; VON WILLEBRAND DISEASE; VON WILLEBRAND FACTOR;

EID: 33644852555     PISSN: 15387933     EISSN: 15387836     Source Type: Journal    
DOI: 10.1111/j.1538-7836.2005.01675.x     Document Type: Article

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