Gene Defects in 150 Unrelated French Cases with Type 2 von Willebrand Disease: from the Patient to the Gene - Meyer, D; Fressinaud, E; Gaucher, C; Lavergne, J-M; Hilbert, L; Ribba, A-S; Jorieux, S; Mazurier, C; INSERM Network on Molecular Abnormalities in von Willebrand Disease (Thrombosis and Haemostasis, 1997)