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Reinvestigation of unidentified causative variants in FXI‐deficient patients: Focus on gene segment deletions von De Mazancourt, Philippe, Harroche, Annie, Pouymayou, Katia, Sigaud, Marianne, Falaise, Céline, Stieltjes, Natalie, Castet, Sabine‐Marie, Tardy, Brigitte, Zawadzki, Christophe, Goudemand, Jenny, Dargaud, Yesim

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Screening platelet function in blood donors von Pedini, Pascal, Baudey, Jean‐Baptiste, Pouymayou, Katia, Falaise, Celine, Ibrahim‐Kosta, Manal, Vélier, Melanie, Demerle, Clémence, Graiet, Hajer, Dragutini, Catherine, Dombey, Anne‐marie, Chiaroni, Jacques, Alessi, Marie Christine, Picard, Christophe

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Impaired dimerization of von Willebrand factor subunit due to mutation A2801D in the CK domain results in a recessive type 2A subtype IID von Willebrand disease von Hommais, Antoine, Stépanian, Alain, Fressinaud, Edith, Mazurier, Claudine, Pouymayou, Katia, Meyer, Dominique, Girma, Jean-Pierre, Ribba, Anne-Sophie

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A Laboratory Phenotype/Genotype Correlation of 1167 French Patients From 670 Families With von Willebrand Disease: A New Epidemiologic Picture von Veyradier, Agnès, Boisseau, Pierre, Fressinaud, Edith, Caron, Claudine, Ternisien, Catherine, Giraud, Mathilde, Zawadzki, Christophe, Trossaert, Marc, Itzhar-Baïkian, Nathalie, Dreyfus, Marie, d'Oiron, Roseline, Borel-Derlon, Annie, Susen, Sophie, Bezieau, Stéphane, Denis, Cécile V, Goudemand, Jenny

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Impaired dimerization of von willebrand factor subunit due to mutation A280 ID in the CK domain results in a recessive type 2A subtype IID von willebrand disease von HOMMAIS, Antoine, STEPANIAN, Alain, FRESSINAUD, Edith, MAZURIER, Claudine, POUYMAYOU, Katia, MEYER, Dominique, GIRMA, Jean-Pierre, RIBBA, Anne-Sophie

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