Prognostic impact of genetic abnormalities in 536 first‐line chronic lymphocytic leukaemia patients without 17p deletion treated with chemoimmunotherapy in two prospective trials:... by Nguyen‐Khac, Florence, Baron, Marine, Guièze, Romain, Feugier, Pierre, Fayault, Alexandra, Raynaud, Sophie, Troussard, Xavier, Droin, Nathalie, Damm, Frederik, Smagghe, Luce, Susin, Santos, Leblond, Véronique, Dartigeas, Caroline, Van den Neste, Eric, Leprêtre, Stéphane, Bernard, Olivier A., Roos‐Weil, Damien

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Cytogenetic and molecular abnormalities in Waldenström's macroglobulinemia patients: Correlations and prognostic impact by Krzisch, Daphné, Guedes, Nayara, Boccon‐Gibod, Clémentine, Baron, Marine, Bravetti, Clotilde, Davi, Frédéric, Armand, Marine, Smagghe, Luce, Caron, Jonathan, Bernard, Olivier A., Susin, Santos, Chapiro, Elise, Leblond, Véronique, Nguyen‐Khac, Florence, Roos‐Weil, Damien

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The t(X;20)(q13;q13) translocation is a good prognostic factor in myeloid neoplasms: A report of 25 cases from the Groupe Francophone de Cytogénétique Hématologique by Nguyen‐Khac, Florence, Muller, Marc, Chapiro, Elise, Abermil, Nassera, Collonge‐Rame, Marie‐Agnes, Daudignon, Agnes, Gaillard, Baptiste, Guzun, Doina, Ittel, Antoine, Lefebvre, Christine, Lesesve, Jean‐Francois, Mozziconacci, Marie‐Joelle, Penther, Dominique, Quessada, Julie, Settegrana, Catherine, Smagghe, Luce, Terre, Christine, Veronese, Lauren, Hirsch, Pierre, Troadec, Marie‐Bérengère

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P596: DELETION OF THE SHORT ARM OF CHROMOSOME 8 AND TNFRSF10B LOSS ASSOCIATE TO POOR PROGNOSIS AND DRUG RESISTANCE IN CHRONIC LYMPHOCYTIC LEUKEMIA by Jondreville, Ludovic, Dehgane, Lea, Doualle, Cecile, Smagghe, Luce, Grange, Beatrice, Davi, Frederic, Koch Lerner, Leticia, Garnier, Delphine, Bravetti, Clotilde, Tournilhac, Olivier, Roos‐Weil, Damien, Boubaya, Marouane, Chapiro, Elise, A Susin, Santos, Nguyen‐Khac, Florence

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del(8p) and TNFRSF10B loss are associated with a poor prognosis and resistance to fludarabine in chronic lymphocytic leukemia by Jondreville, Ludovic, Dehgane, Lea, Doualle, Cecile, Smagghe, Luce, Grange, Beatrice, Davi, Frederic, Lerner, Leticia K., Garnier, Delphine, Bravetti, Clotilde, Tournilhac, Olivier, Roos-Weil, Damien, Boubaya, Marouane, Chapiro, Elise, Susin, Santos A., Nguyen-Khac, Florence

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An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients by Bonnet, Crystel, Riahi, Zied, Chantot-Bastaraud, Sandra, Smagghe, Luce, Letexier, Mélanie, Marcaillou, Charles, Lefèvre, Gaëlle M, Hardelin, Jean-Pierre, El-Amraoui, Aziz, Singh-Estivalet, Amrit, Mohand-Saïd, Saddek, Kohl, Susanne, Kurtenbach, Anne, Sliesoraityte, Ieva, Zobor, Ditta, Gherbi, Souad, Testa, Francesco, Simonelli, Francesca, Banfi, Sandro, Fakin, Ana, Glavač, Damjan, Jarc-Vidmar, Martina, Zupan, Andrej, Battelino, Saba, Martorell Sampol, Loreto, Claveria, Maria Antonia, Catala Mora, Jaume, Dad, Shzeena, Møller, Lisbeth B, Rodriguez Jorge, Jesus, Hawlina, Marko, Auricchio, Alberto, Sahel, José-Alain, Marlin, Sandrine, Zrenner, Eberhart, Audo, Isabelle, Petit, Christine

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Cytogenetic and molecular abnormalities in W aldenström's macroglobulinemia patients: Correlations and prognostic impact by Krzisch, Daphné, Guedes, Nayara, Boccon‐Gibod, Clémentine, Baron, Marine, Bravetti, Clotilde, Davi, Frédéric, Armand, Marine, Smagghe, Luce, Caron, Jonathan, Bernard, Olivier A., Susin, Santos, Chapiro, Elise, Leblond, Véronique, Nguyen‐Khac, Florence, Roos‐Weil, Damien

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