Differentiating Among Delinquent, At-Risk, and Not At-Risk Adolescents Using a Multidimensional Model of Self-Concept von Bianco, Tania Marie, Houghton, Stephen, French, Davina, Fernandez, Miguel

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The wide spectrum of tubulinopathies: what are the key features for the diagnosis? von BAHI-BUISSON, Nadia, POIRIER, Karine, LASCELLES, Karine, SOUVILLE, Isabelle, BELDJORD, Cherif, CHELLY, Jamel, FOURNIOL, Franck, SAILLOUR, Yoann, VALENCE, Stéphanie, LEBRUN, Nicolas, HULLY, Marie, BIANCO, Catherine Fallet, BODDAERT, Nathalie, ELIE, Caroline

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Identification of Mutations in TMEM5 and ISPD as a Cause of Severe Cobblestone Lissencephaly von Vuillaumier-Barrot, Sandrine, Bouchet-Séraphin, Céline, Chelbi, Malika, Devisme, Louise, Quentin, Samuel, Gazal, Steven, Laquerrière, Annie, Fallet-Bianco, Catherine, Loget, Philippe, Odent, Sylvie, Carles, Dominique, Bazin, Anne, Aziza, Jacqueline, Clemenson, Alix, Guimiot, Fabien, Bonnière, Maryse, Monnot, Sophie, Bole-Feysot, Christine, Bernard, Jean-Pierre, Loeuillet, Laurence, Gonzales, Marie, Socha, Koryna, Grandchamp, Bernard, Attié-Bitach, Tania, Encha-Razavi, Férechté, Seta, Nathalie

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Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies von Devisme, Louise, Bouchet, Céline, Gonzalès, Marie, Alanio, Elisabeth, Bazin, Anne, Bessières, Bettina, Bigi, Nicole, Blanchet, Patricia, Bonneau, Dominique, Bonnières, Maryse, Bucourt, Martine, Carles, Dominique, Clarisse, Bénedicte, Delahaye, Sophie, Fallet-Bianco, Catherine, Figarella-Branger, Dominique, Gaillard, Dominique, Gasser, Bernard, Delezoide, Anne-Lise, Guimiot, Fabien, Joubert, Madeleine, Laurent, Nicole, Laquerrière, Annie, Liprandi, Agnès, Loget, Philippe, Marcorelles, Pascale, Martinovic, Jelena, Menez, Francoise, Patrier, Sophie, Pelluard, Fanny, Perez, Marie-José, Rouleau, Caroline, Triau, Stéphane, Attié-Bitach, Tania, Vuillaumier-Barrot, Sandrine, Seta, Nathalie, Encha-Razavi, Férechté

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Clinical and molecular data in cases of prenatal localized overgrowth disorder: major implication of genetic variants in PI3K‐AKT‐mTOR signaling pathway von Bourgon, N., Carmignac, V., Sorlin, A., Duffourd, Y., Philippe, C., Thauvin‐Robinet, C., Guibaud, L., Faivre, L., Vabres, P., Kuentz, P., Tisserand, Emilie, Chevarin, Martin, Delanne, Julian, Jouan, Thibaud, Pöe, Charlotte, Abel, Carine, Allory, Patrick, Amram, Daniel, Attie‐Bitach, Tania, Aziza, Jacqueline, Benevent, Jean‐Baptiste, Bidat, Laurent, Bessières, Bettina, Boussion, Françoise, Cabaret‐Dufour, Anne‐Sophie, Chanoz‐Poulard, Geneviève, Chassaing, Nicolas, Ciorna‐Monferrato, Viorica, Cordier, Anne‐Gaëlle, Cordier, Marie‐Pierre, Cuillier, Fabrice, Doray, Berenice, Encha‐Razavi, Ferechte, Eszto, Marie‐Laure, Bianco, Catherine Fallet, Fernandez, Carla, Ferry, Mathilde, Fichez, Axel, Vequeau, Valérie Goua, Grevent, David, Guichet, Agnès, Laurent, Nicole, Le Gac, Marie‐Pascale, Lefebvre, Mathilde, Letard, Pascaline, Loget, Philippe, Loisel, Didier, Martinovich, Jelena, Masutti, Jean‐Paul, Millischer, Anne‐Elodie, Musizzano, Yuri, Nord, Jean‐François, Perez, Marie‐Josée, Prieur, Fabienne, Proisy, Maia, Quelin, Chloé, Roth, Philippe, Rousseau, Thierry, Salomon, Laurent, Sonigo, Pascale, Spaggiari, Emmanuel, Stempfle, Noëlle, Stirnemann, Julien, Tanteau, Julia, Triau, Stéphane, Vasiljevic, Alexandre, Ville, Yves, Zidane‐Marinnes, Merzouka, Kaltenbach, Sophie, Rivière, Jean‐Baptiste

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Antenatal spectrum of CHARGE syndrome in 40 fetuses with CHD7 mutations von Legendre, Marine, Gonzales, Marie, Goudefroye, Géraldine, Bilan, Frédéric, Parisot, Pauline, Perez, Marie-José, Bonnière, Maryse, Bessières, Bettina, Martinovic, Jelena, Delezoide, Anne-Lise, Jossic, Frédérique, Fallet-Bianco, Catherine, Bucourt, Martine, Tantau, Julia, Loget, Philippe, Loeuillet, Laurence, Laurent, Nicole, Leroy, Brigitte, Salhi, Houria, Bigi, Nicole, Rouleau, Caroline, Guimiot, Fabien, Quélin, Chloé, Bazin, Anne, Alby, Caroline, Ichkou, Amale, Gesny, Roselyne, Kitzis, Alain, Ville, Yves, Lyonnet, Stanislas, Razavi, Ferechte, Gilbert-Dussardier, Brigitte, Vekemans, Michel, Attié-Bitach, Tania

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Matthew-Wood syndrome: Report of two new cases supporting autosomal recessive inheritance and exclusion of FGF10 and FGFR2 von Martinovic-Bouriel, Jelena, Bernabé-Dupont, Céline, Golzio, Christelle, Grattagliano-Bessières, Bettina, Malan, Valérie, Bonnière, Maryse, Esculpavit, Chantal, Fallet-Bianco, Catherine, Mirlesse, Véronique, Le Bidois, Jerôme, Aubry, Marie-Cécile, Vekemans, Michel, Morichon, Nicole, Etchevers, Heather, Attié-Bitach, Tania, Encha-Razavi, Féréchté, Benachi, Alexandra

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