المؤلفون: Tricoche, Leslie, Pélisson, Denis, Longo, Léa, Koun, Eric, Poisson, Alice, Prado, Jérôme, Meunier, Martine

المصدر: In NeuroImage 15 August 2023 277

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المؤلفون: Zawerton, Ash, Mignot, Cyril, Sigafoos, Ashley, Blackburn, Patrick R, Haseeb, Abdul, McWalter, Kirsty, Ichikawa, Shoji, Nava, Caroline, Keren, Boris, Charles, Perrine, Marey, Isabelle, Tabet, Anne-Claude, Levy, Jonathan, Perrin, Laurence, Hartmann, Andreas, Lesca, Gaetan, Schluth-Bolard, Caroline, Monin, Pauline, Dupuis-Girod, Sophie, Guillen Sacoto, Maria J, Schnur, Rhonda E, Zhu, Zehua, Poisson, Alice, El Chehadeh, Salima, Alembik, Yves, Bruel, Ange-Line, Lehalle, Daphné, Nambot, Sophie, Moutton, Sébastien, Odent, Sylvie, Jaillard, Sylvie, Dubourg, Christèle, Hilhorst-Hofstee, Yvonne, Barbaro-Dieber, Tina, Ortega, Lucia, Bhoj, Elizabeth J, Masser-Frye, Diane, Bird, Lynne M, Lindstrom, Kristin, Ramsey, Keri M, Narayanan, Vinodh, Fassi, Emily, Willing, Marcia, Cole, Trevor, Salter, Claire G, Akilapa, Rhoda, Vandersteen, Anthony, Canham, Natalie, Rump, Patrick, Gerkes, Erica H, Klein Wassink-Ruiter, Jolien S, Bijlsma, Emilia, Hoffer, Mariëtte JV, Vargas, Marcelo, Wojcik, Antonina, Cherik, Florian, Francannet, Christine, Rosenfeld, Jill A, Machol, Keren, Scott, Daryl A, Bacino, Carlos A, Wang, Xia, Clark, Gary D, Bertoli, Marta, Zwolinski, Simon, Thomas, Rhys H, Akay, Ela, Chang, Richard C, Bressi, Rebekah, Sanchez Russo, Rossana, Srour, Myriam, Russell, Laura, Goyette, Anne-Marie E, Dupuis, Lucie, Mendoza-Londono, Roberto, Karimov, Catherine, Joseph, Maries, Nizon, Mathilde, Cogné, Benjamin, Kuechler, Alma, Piton, Amélie, Klee, Eric W, Lefebvre, Véronique, Clark, Karl J, Depienne, Christel

المصدر: Genetics in Medicine. 22(3)

مصطلحات موضوعية: Intellectual and Developmental Disabilities (IDD), Pediatric, Genetics, Brain Disorders, Clinical Research, Rare Diseases, Human Genome, Aetiology, 2.1 Biological and endogenous factors, Adolescent, Adult, Animals, Child, Child, Preschool, DNA-Binding Proteins, Female, Genetic Predisposition to Disease, Haploinsufficiency, Humans, Infant, Intellectual Disability, Language Development Disorders, Male, Mutation, Missense, Neurodevelopmental Disorders, Pedigree, Phenotype, SOXD Transcription Factors, Young Adult, autism, developmental delay, intellectual disability, epilepsy, missense variants, Deciphering Developmental DisorderStudy, missense variants., Clinical Sciences, Genetics & Heredity

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/14x4x4wp

المؤلفون: Bar, Claire, Breuillard, Delphine, Kuchenbuch, Mathieu, Jennesson, Mélanie, Le Guyader, Gwenaël, Isnard, Hervé, Rolland, Anne, Doummar, Diane, Fluss, Joel, Afenjar, Alexandra, Berquin, Patrick, De Saint Martin, Anne, Dupont, Sophie, Goldenberg, Alice, Lederer, Damien, Lesca, Gaétan, Maurey, Hélène, Meyer, Pierre, Mignot, Cyril, Nica, Anca, Odent, Sylvie, Poisson, Alice, Scalais, Emmanuel, Sekhara, Tayeb, Vrielynck, Pascal, Barcia, Giulia, Nabbout, Rima

المصدر: In Epilepsy & Behavior January 2022 126

المؤلفون: Harris, Holly K.^{Aff1, Aff2}, Nakayama, Tojo^{Aff3, Aff4}, Lai, Jenny^{Aff3, Aff5}, Zhao, Boxun^{Aff3, Aff4}, Argyrou, Nikoleta^{Aff3, Aff4}, Gubbels, Cynthia S.^{Aff3, Aff4}, Soucy, Aubrie^{Aff3, Aff4}, Genetti, Casie A.^{Aff3, Aff4}, Suslovitch, Victoria^{Aff3, Aff4}, Rodan, Lance H.^{Aff3, Aff4, Aff6}, Tiller, George E., Lesca, Gaetan, Gripp, Karen W., Asadollahi, Reza, Hamosh, Ada, Applegate, Carolyn D., Turnpenny, Peter D., Simon, Marleen E. H., Volker-Touw, Catharina M. L., Gassen, Koen L. I. van, Binsbergen, Ellen van, Pfundt, Rolph, Gardeitchik, Thatjana, Vries, Bert B. A. de, Immken, LaDonna L., Buchanan, Catherine, Willing, Marcia, Toler, Tomi L., Fassi, Emily, Baker, Laura, Vansenne, Fleur, Wang, Xiadong, Ambrus, Jr., Julian L., Fannemel, Madeleine, Posey, Jennifer E., Agolini, Emanuele, Novelli, Antonio, Rauch, Anita, Boonsawat, Paranchai, Fagerberg, Christina R., Larsen, Martin J., Kibaek, Maria, Labalme, Audrey, Poisson, Alice, Payne, Katelyn K., Walsh, Laurence E.^{Aff24, Aff25}, Aldinger, Kimberly A., Balciuniene, Jorune, Skraban, Cara, Gray, Christopher, Murrell, Jill, Bupp, Caleb P., Pascolini, Giulia, Grammatico, Paola, Broly, Martin, Küry, Sébastien, Nizon, Mathilde, Rasool, Iqra Ghulam^{Aff31, Aff32}, Zahoor, Muhammad Yasir, Kraus, Cornelia, Reis, André, Iqbal, Muhammad, Uguen, Kevin^{Aff34, Aff35}, Audebert-Bellanger, Severine, Ferec, Claude^{Aff34, Aff35}, Redon, Sylvia^{Aff34, Aff35}, Baker, Janice, Wu, Yunhong, Zampino, Guiseppe, Syrbe, Steffan, Brosse, Ines, Jamra, Rami Abou, Dobyns, William B., Cohen, Lilian L., Blomhoff, Anne, Mignot, Cyril^{Aff43, Aff44}, Keren, Boris, Courtin, Thomas, Agrawal, Pankaj B.^{Aff3, Aff4}, Beggs, Alan H.^{Aff3, Aff4}, Yu, Timothy W.^{Aff3, Aff4, Aff5}

المصدر: Genetics in Medicine: Official journal of the American College of Medical Genetics and Genomics. 23(6):1028-1040

المؤلفون: Demily, Caroline, Lesca, Gaétan, Poisson, Alice, Till, Marianne, Barcia, Giulia, Chatron, Nicolas, Sanlaville, Damien, Munnich, Arnold

المصدر: Journal of Autism and Developmental Disorders. Aug 2018 48(8):2886-2889.

Peer Reviewed: Y

Page Count: 4

Descriptors: Autism, Pervasive Developmental Disorders, Genetics, Epilepsy, Duplication, Pathology, Counseling

المؤلفون: GAULD, Christophe^{Aff1, Aff2}, POISSON, Alice, REVERSAT, Julie, PEYROUX, Elodie, HOUDAYER-ROBERT, Françoise, ROSSI, Massimiliano, LESCA, Gaetan, SANLAVILLE, Damien^{Aff5, Aff6}, DEMILY, Caroline^{Aff3, Aff7}

المصدر: BMC Psychiatry. 21(1)

المؤلفون: Schwartz, Flora, Epinat-Duclos, Justine, Léone, Jessica, Poisson, Alice, Prado, Jérôme

المصدر: In Neuropsychologia April 2020 141

المؤلفون: Demily, Caroline^Aff1, Lesca, Gaétan^{Aff2, Aff3}, Poisson, Alice, Till, Marianne, Barcia, Giulia, Chatron, Nicolas^{Aff2, Aff3}, Sanlaville, Damien^{Aff2, Aff3}, Munnich, Arnold

المصدر: Journal of Autism and Developmental Disorders. 48(8):2886-2889

المؤلفون: Poisson, Alice^Aff1, Chatron, Nicolas, Labalme, Audrey, Fourneret, Pierre^{Aff3, Aff4, Aff5}, Ville, Dorothée, Mathieu, Marie Laure^{Aff7, Aff8}, Sanlaville, Damien, Demily, Caroline, Lesca, Gaëtan

المصدر: BMC Medical Genetics. 21(1)