Are all Xq26.2 duplications overlapping GPC3 on array‐CGH a cause of Simpson‐Golabi‐Behmel syndrome? When do we need transcript analysis? by 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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Aarskog-Scott syndrome: first report of a duplication in the FGD1 gene by Ronce, N, Maystadt, I, Hubert, C, Vonwill, S, Devriendt, K, Moizard, M-P, Raynaud, M

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Phenotype and genotype in females with POU3F4 mutations by Marlin, S, Moizard, MP, David, A, Chaissang, N, Raynaud, M, Jonard, L, Feldmann, D, Loundon, N, Denoyelle, F, Toutain, 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 by 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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Twenty-five novel mutations including duplications in the ATP7A gene by 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 by 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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A C2055T Transition in Exon 8 of the ATP7A Gene Is Associated with Exon Skipping in an Occipital Horn Syndrome Family by Ronce, Nathalie, Moizard, Marie-Pierre, Robb, Laura, Toutain, Annick, Villard, Laurent, Moraine, Claude

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Are Dp71 and Dp140 brain dystrophin isoforms related to cognitive impairment in Duchenne muscular dystrophy? by Moizard, Marie-Pierre, Billard, Catherine, Toutain, Annick, Berret, Françoise, Marmin, Nadine, Moraine, Claude

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Evidence for a new X-linked mental retardation gene in Xp21-Xp22: Clinical and molecular data in one family by Ronce, Nathalie, Raynaud, Martine, Toutain, Annick, Moizard, Marie-Pierre, Colleaux, Laurence, Gendrot, Chantal, Briault, Sylvain, Moraine, Claude

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Phenotype and genotype in females with PO U3F4 mutations by MARLIN, S, MOIZARD, M. P, DAVID, A, CHAISSANG, N, RAYNAUD, M, JONARD, L, FELDMANN, D, LOUNDON, N, DENOYELLE, F, TOUTAIN, A

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

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In-frame deletion in MECP2 causes mild nonspecific mental retardation by Yntema, Helger G., Oudakker, Astrid R., Kleefstra, Tjitske, Hamel, Ben C.J., van Bokhoven, Hans, Chelly, Jamel, Kalscheuer, Vera M., Fryns, Jean-Pierre, Raynaud, Martine, Moizard, Marie-Pierre, Moraine, Claude

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Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX consortium by 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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