Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian type 1 VWD study.

James, P D; Paterson, A D; Notley, C; Cameron, C; Hegadorn, C; Tinlin, S; Brown, C; O'Brien, L; Leggo, J; Lillicrap, D

James, P D; Paterson, A D; Notley, C; Cameron, C; Hegadorn, C; Tinlin, S; Brown, C; O'Brien, L; Leggo, J; Lillicrap, D.

Affiliation

James PD; Department of Medicine, Queen's University, Kingston, Canada.

J Thromb Haemost ; 4(4): 783-92, 2006 Apr.

Article in En | MEDLINE | ID: mdl-16634747

Subject(s)

Genetic Linkage; von Willebrand Diseases/genetics; ABO Blood-Group System; Adolescent; Adult; Canada; Child; Child, Preschool; Family Health; Genetic Variation; Humans; Infant; Infant, Newborn; Middle Aged; Phenotype; von Willebrand Factor/genetics

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Collection: 01-internacional Database: MEDLINE Main subject: Von Willebrand Diseases / Genetic Linkage Type of study: Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Humans / Infant / Middle aged / Newborn Country/Region as subject: America do norte Language: En Journal: J Thromb Haemost Journal subject: HEMATOLOGIA Year: 2006 Type: Article Affiliation country: Canada

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