SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development von Young, Jacques, Metay, Corinne, Bouligand, Jerome, Tou, Bassim, Francou, Bruno, Maione, Luigi, Tosca, Lucie, Sarfati, Julie, Brioude, Frédéric, Esteva, Blandine, Briand-Suleau, Audrey, Brisset, Sophie, Goossens, Michel, Tachdjian, Gerard, Guiochon-Mantel, Anne

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Iron Overload Exacerbates Busulfan-Melphalan Toxicity Through a Pharmacodynamic Interaction in Mice von Bouligand, Jérôme, Richard, Clémentine, Valteau-Couanet, Dominique, Orear, Cedric, Mercier, Lionel, Kessari, Romain, Simonnard, Nicolas, Munier, Fabienne, Daudigeos-Dubus, Estelle, Tou, Bassim, Opolon, Paule, Deroussent, Alain, Paci, Angelo, Vassal, Gilles

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Molecular characterization of 1q44 microdeletion in 11 patients reveals three candidate genes for intellectual disability and seizures von Thierry, Gaelle, Bénéteau, Claire, Pichon, Olivier, Flori, Elisabeth, Isidor, Bertrand, Popelard, Françoise, Delrue, Marie-Ange, Duboscq-Bidot, Laetitia, Thuresson, Ann-Charlotte, van Bon, Bregje W.M., Cailley, Dorothée, Rooryck, Caroline, Paubel, Agathe, Metay, Corinne, Dusser, Anne, Pasquier, Laurent, Béri, Mylène, Bonnet, Céline, Jaillard, Sylvie, Dubourg, Christèle, Tou, Bassim, Quéré, Marie-Pierre, Soussi-Zander, Cecilia, Toutain, Annick, Lacombe, Didier, Arveiler, Benoit, de Vries, Bert B.A., Jonveaux, Philippe, David, Albert, Le Caignec, Cédric

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SALL4 and NFATC2: two major actors of interstitial 20q13.2 duplication: Genotype-phenotype relevance in 20q13.2 gain von Briand-Suleau, Audrey, Martinovic, Jelena, Tosca, Lucie, Tou, Bassim, Brisset, Sophie, Bouligand, Jérôme, Delattre, Valérie, Giurgea, Irina, Bachir, J., Folliot, P., Goumy, Carole, Francannet, Christine, Guiochon-Mantel, Anne, Benachi, Alexandra, Vermeesch, J., Tachdjian, Gérard, Vago, Philippe, Goossens, Michel, Métay, Corinne

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