Ten candidate ADAMTS13 mutations in six French families with congenital thrombotic thrombocytopenic purpura (Upshaw–Schulman syndrome) von Veyradier, A., Lavergne, J‐M., Ribba, A‐S., Obert, B., Loirat, C., Meyer, D., Girma, J‐P.

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Molecular characterization of Iranian patients with type 3 von Willebrand disease von SHAHBAZI, S., MAHDIAN, R., ALA, F. A., LAVERGNE, J.-M., DENIS, C. V., CHRISTOPHE, O. D.

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Somatic Mosaicism in Hemophilia A: A Fairly Common Event von Leuer, Marco, Oldenburg, Johannes, Lavergne, Jean-Maurice, Ludwig, Michael, Fregin, Andreas, Eigel, Anton, Ljung, Rolf, Goodeve, Anne, Peake, Ian, Olek, Klaus

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Occurrence of myeloproliferative disorder in patients with Noonan syndrome von Bader-Meunier, B., Tchernia, G., Miélot, F., Fontaine, J.L., Thomas, C., Lyonnet, S., Lavergne, J.M., Dommergues, J.P.

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Ser968Thr Mutation within the A3 Domain of Von Willebrand Factor (VWF) in Two Related Patients Leads to a Defective Binding of VWF to Collagen von Ribba, Anne-Sophie, Loisel, Irmine, Lavergne, Jean-Maurice, Juhan-Vague, Irène, Obert, Bernadette, Cherel, Ghislaine, Meyer, Dominique, Girma, Jean-Pierre

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Fast and Efficient Mutation Detection Method Using Multiplex PCR and Cycle Sequencing Application to Haemophilia B von COSTA, J. M, ERNAULT, P, VIDAUD, D, VIDAUD, M, MEYER, D, LAVERGNE, J. M

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Factor VIII (FVIII) gene mutations in 120 patients with hemophilia A: detection of 26 novel mutations and correlation with FVIII inhibitor development von REPESSÉ, Y., SLAOUI, M., FERRANDIZ, D., GAUTIER, P., COSTA, C., COSTA, J. M., LAVERGNE, J. M., BOREL‐DERLON, A.

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Identification of intron 1 and 22 inversion mutations in the factor VIII gene of 124 Iranian families with severe haemophilia A von Rastegar lari, G., Enayat, M. S., Arjang, Z., Lavergne, J. M., Ala, F.

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Factor VIII genotype and inhibitor development in patients with haemophilia A: highest risk in patients with splice site mutations von BOEKHORST, J., LARI, G. R., D'OIRON, R., COSTA, J. M., NOVÁKOVÁ, I. R. O., ALA, F. A., LAVERGNE, J. M., VAN HEERDE, W. L.

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Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition von Tuddenham, E.G.D., Schwaab, R., Seehafer, J., Millar, D.S., Gitschier, J., Higuchi, M., Bidichandani, S., Connor, J.M., Hoyer, L.W., Yoshioka, A., Peake, I.R., Olek, K., Kazazian, H.H., Lavergne, J.-M., Giannelli, F., Antonarakis, S.E., Cooper, D.N.

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Discrepancy Between IIA Phenotype and IIB Genotype in a Patient With a Variant of von Willebrand Disease von Ribba, A.S., Christophe, O., Derlon, A., Cherel, G., Siguret, V., Lavergne, J.M., Girma, J.P., Meyer, D., Pietu, G.

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Mutations in the catalytic domain of human coagulation factor IX: Rapid characterization by direct genomic sequencing of DNA fragments displaying an altered melting behavior von Attree, Oliver, Vidaud, Dominique, Vidaud, Michel, Amselem, Serge, Lavergne, Jean-Maurice, Goossens, Michel

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A patient with type 2N von Willebrand disease is heterozygous for a new mutation: Gly22Glu. Demonstration of a defective expression of the second allele by the use of monoclonal an... von GU, J, JORIEUX, S, LAVERGNE, J. M, RUAN, C, MAZURIER, C, MEYER, D

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Mild haemophilia A discovered in a previously multi‐operated 73‐year‐old man: characterization of a new mutation von Bauduer, F., Ducout, L., Bendriss, P., Falaises, B., Lavergne, J. M.

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Comparison of the primary structure of the functional domains of human and porcine von Willebrand factor that mediate platelet adhesion von Bahnak, Bruce R., Lavergne, Jean-Maurice, Ferreira, Valérie, Kerbiriou-Nabias, Danièle, Meyer, Dominique

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The arginine-552-cysteine (R1315C) mutation within the A1 loop of von Willebrand factor induces an abnormal folding with a loss of function resulting in type 2A-like phenotype of v... von RIBBA, Anne-Sophie, HILBERT, Lysiane, MEYER, Dominique, LAVERGNE, Jean-Maurice, FRESSINAUD, Edith, BOYER-NEUMANN, Catherine, TERNISIEN, Catherine, JUHAN-VAGUE, Irène, GOUDEMAND, Jenny, GIRMA, Jean-Pierre, MAZURIER, Claudine

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Duplication of a methionine within the glycoprotein Ib binding domain of von Willebrand factor detected by denaturing gradient gel electrophoresis in a patient with type IIB von Wi... von RIBBA, A. S, LAVERGNE, J. M, BAHNAK, B. R, DERLON, A, PIETU, G, MEYER, D

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Functional mapping of anti–factor IX inhibitors developed in patients with severe hemophilia B von Christophe, Olivier D., Lenting, Peter J., Cherel, Ghislaine, Boon-Spijker, Mariette, Lavergne, Jean-Maurice, Boertjes, Ria, Briquel, Marie-Elisabeth, de Goede-Bolder, Arja, Goudemand, Jenny, Gaillard, Solange, d'Oiron, Roseline, Meyer, Dominique, Mertens, Koen

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Myelodysplasia in childhood may be a polyclonal disease von TCHERNIA, G, BADER-MEUNIER, B, LAVERGNE, J. M, MIELOT, F, DOMMERGUES, J. P

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Additional translocation (9;12)(p13;q24.1) in newly diagnosed chronic myeloid leukemia : complete cytogenetic remission after interferon therapy von TERTIAN, G, AVALOS, M. R, LEONARD, C, LAVERGNE, J. M, MISRAHI, M, TCHERNIA, G

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