Intérêt des dosages des métabolites actifs dans le suivi du traitement par azathioprine pour maladie de Crohn von CAGNARD, B, TOSONI-VERLINGUE, D, TRIBUT, O, MOIZARD, C, BRIDOUX-HENNO, L, DELAPERRIERE, N, BENTUE-FERRER, D, DABADIE, A

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Advantages of different dosages of active metabolites in the follow-up of azathioprine treatment for Crohn disease von Cagnard, B, Tosoni-Verlingue, D, Tribut, O, Moizard, C, Bridoux-Henno, L, Delaperriere, N, Bentue-Ferrer, D, Dabadie, A

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X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family von Laumonnier, Frédéric, Bonnet-Brilhault, Frédérique, Gomot, Marie, Blanc, Romuald, David, Albert, Moizard, Marie-Pierre, Raynaud, Martine, Ronce, Nathalie, Lemonnier, Eric, Calvas, Patrick, Laudier, Béatrice, Chelly, Jamel, Fryns, Jean-Pierre, Ropers, Hans-Hilger, Hamel, Ben C.J., Andres, Christian, Barthélémy, Catherine, Moraine, Claude, Briault, Sylvain

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Are all Xq26.2 duplications overlapping GPC3 on array‐CGH a cause of Simpson‐Golabi‐Behmel syndrome? When do we need transcript analysis? von Vuillaume, M.‐L., Moizard, M.‐P., Hammouche, E., Delrue, M.‐A., Perrin, L., Maftei, C., Dupont, C., Drunat, S., Cottereau, E., Baumann, C., Toutain, A.

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Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth von Jeanne, Médéric, Vuillaume, Marie-Laure, Ung, Dévina C., Vancollie, Valerie E., Wagner, Christel, Collins, Stephan C., Vonwill, Sandrine, Haye, Damien, Chelloug, Nora, Pfundt, Rolph, Kummeling, Joost, Moizard, Marie-Pierre, Marouillat, Sylviane, Kleefstra, Tjitske, Yalcin, Binnaz, Laumonnier, Frédéric, Toutain, Annick

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La mobilisation contentieuse limitée de la discrimination au travail en raison des convictions religieuses von Moizard, Nicolas

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Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX consortium von de Brouwer, Arjan P.M., Yntema, Helger G., Kleefstra, Tjitske, Lugtenberg, Dorien, Oudakker, Astrid R., de Vries, Bert B.A., van Bokhoven, Hans, Van Esch, Hilde, Frints, Suzanne G.M., Froyen, Guy, Fryns, Jean-Pierre, Raynaud, Martine, Moizard, Marie-Pierre, Ronce, Nathalie, Bensalem, Anissa, Moraine, Claude, Poirier, Karine, Castelnau, Laetitia, Saillour, Yoann, Bienvenu, Thierry, Beldjord, Chérif, des Portes, Vincent, Chelly, Jamel, Turner, Gillian, Fullston, Tod, Gecz, Jozef, Kuss, Andreas W., Tzschach, Andreas, Jensen, Lars Riff, Lenzner, Steffen, Kalscheuer, Vera M., Ropers, Hans-Hilger, Hamel, Ben C.J.

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FACL4 , encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation von Bellan, Cristina, des Portes, Vincent, Lewis, Sarah E, Yntema, Helger G, Muscettola, Maddalena, Fryns, Jean-Pierre, Schaffer, Jean E, Longo, Ilaria, Raynaud, Martine, Moizard, Marie-Pierre, Volpi, Nila, Meloni, Ilaria, Magi, Barbara, Gomot, Marie, Chelly, Jamel, Ropers, Hans-Hilger, Bruttini, Mirella, Renieri, Alessandra

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Aarskog-Scott syndrome: first report of a duplication in the FGD1 gene von Ronce, N, Maystadt, I, Hubert, C, Vonwill, S, Devriendt, K, Moizard, M-P, Raynaud, M

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Les sciences citoyennes à l’ère de la santé numérique von Moizard-Lanvin, Justyna

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Sandrine Turgis (dir.), Les données numériques des migrants et des réfugiés sous l’angle du droit européen, Presses universitaires de Rennes, 2020, 236 p von Haguenau-Moizard, Catherine

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Sélectionner et agréger les ignorances von Moizard-Lanvin, Justyna

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Severe cognitive impairment in DMD: obvious clinical indication for Dp71 isoform point mutation screening von Moizard, M P, Toutain, A, Fournier, D, Berret, F, Raynaud, M, Billard, C, Andres, C, Moraine, C

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Twenty‐five novel mutations including duplications in the ATP7A gene von Moizard, M‐P, Ronce, N, Blesson, S, Bieth, E, Burglen, L, Mignot, C, Mortemousque, I, Marmin, N, Dessay, B, Danesino, C, Feillet, F, Castelnau, P, Toutain, A, Moraine, C, Raynaud, M

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Twenty-five novel mutations including duplications in the ATP7A gene von Moizard, M-P, Ronce, N, Blesson, S, Bieth, E, Burglen, L, Mignot, C, Mortemousque, I, Marmin, N, Dessay, B, Danesino, C, Feillet, F, Castelnau, P, Toutain, A, Moraine, C, Raynaud, M

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Aarskog-Scott syndrome: first report of a duplication in the FGD1 gene von Ronce, N, Maystadt, I, Hubert, C, Vonwill, S, Devriendt, Koenraad, Moizard, M.-P, Raynaud, M

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X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes von Hu, H, Haas, S.A, Chelly, J, Van Esch, Hilde, Raynaud, M, de Brouwer, A.P.M, Weinert, S, Froyen, Guy, Frints, S.G.M, Laumonnier, F, Zemojtel, T, Love, M.I, Richard, H, Emde, A.-K, Bienek, M, Jensen, C, Hambrock, M, Fischer, U, Langnick, C, Feldkamp, M, Wissink-Lindhout, W, Lebrun, N, Castelnau, L, Rucci, J, Montjean, R, Dorseuil, O, Billuart, P, Stuhlmann, T, Shaw, M, Corbett, M.A, Gardner, A, Willis-Owen, S, Tan, C, Friend, K.L, Belet, S, van Roozendaal, K.E.P, Jimenez-Pocquet, M, Moizard, M.-P, Ronce, N, Sun, R, O'Keeffe, S, Chenna, R, van Bömmel, A, Göke, J, Hackett, A, Field, M, Christie, L, Boyle, J, Haan, E, Nelson, J, Turner, G, Baynam, G, Gillessen-Kaesbach, G, Müller, U, Steinberger, D, Budny, B, Badura-Stronka, M, Latos-Bieleńska, A, Ousager, L.B, Wieacker, P, Rodríguez Criado, G, Bondeson, M.-L, Annerén, G, Dufke, A, Cohen, M, Van Maldergem, L, Vincent-Delorme, C, Echenne, B, Simon-Bouy, B, Kleefstra, T, Willemsen, M, Fryns, Jean-Pierre, Devriendt, Koenraad, Ullmann, R, Vingron, M, Wrogemann, K, Wienker, T.F, Tzschach, A, van Bokhoven, H, Gecz, J, Jentsch, T.J, Chen, W, Ropers, H.-H, Kalscheuer, V.M

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Ignorance(s) von Barbier, Laura, Boudia, Soraya, Goumri, Maël, Moizard-Lanvin, Justyna

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Ignorance. Widening the focus von Barbier, Laura, Boudia, Soraya, Goumri, Maël, Moizard-Lanvin, Justyna

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X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes von Hu, H, Haas, SA, Chelly, J, Van Esch, H, Raynaud, M, De Brouwer, APM, Weinert, S, Froyen, G, Frints, SGM, Laumonnier, F, Zemojtel, T, Love, MI, Richard, H, Emde, A-K, Bienek, M, Jensen, C, Hambrock, M, Fischer, U, Langnick, C, Feldkamp, M, Wissink-Lindhout, W, Lebrun, N, Castelnau, L, Rucci, J, Montjean, R, Dorseuil, O, Billuart, P, Stuhlmann, T, Shaw, M, Corbett, MA, Gardner, A, Willis-Owen, S, Tan, C, Friend, KL, Belet, S, Van Roozendaal, KEP, Jimenez-Pocquet, M, Moizard, M-P, Ronce, N, Sun, R, O'Keeffe, S, Chenna, R, Van Boemmel, A, Goeke, J, Hackett, A, Field, M, Christie, L, Boyle, J, Haan, E, Nelson, J, Turner, G, Baynam, G, Gillessen-Kaesbach, G, Mueller, U, Steinberger, D, Budny, B, Badura-Stronka, M, Latos-Bielenska, A, Ousager, LB, Wieacker, P, Criado, GR, Bondeson, M-L, Anneren, G, Dufke, A, Cohen, M, Van Maldergem, L, Vincent-Delorme, C, Echenne, B, Simon-Bouy, B, Kleefstra, T, Willemsen, M, Fryns, J-P, Devriendt, K, Ullmann, R, Vingron, M, Wrogemann, K, Wienker, TF, Tzschach, A, Van Bokhoven, H, Gecz, J, Jentsch, TJ, Chen, W, Ropers, H-H, Kalscheuer, VM

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