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1 Ergebnisse
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Convergence of Genes and Cellular Pathways Dysregulated in ..:
Pinto, Dalila
;
Delaby, Elsa
;
Merico, Daniele
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2014.03.018. , 2014
Link:
https://inserm.hal.science/inserm-00986225
RT Journal T1
Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
UL https://suche.suub.uni-bremen.de/peid=base-ftunivtoulouse2:oai:HAL:inserm-00986225v1&Exemplar=1&LAN=DE A1 Pinto, Dalila A1 Delaby, Elsa A1 Merico, Daniele A1 Barbosa, Mafalda A1 Merikangas, Alison A1 Klei, Lambertus A1 Thiruvahindrapuram, Bhooma A1 Xu, Xiao A1 Ziman, Robert A1 Wang, Zhuozhi A1 Vorstman, Jacob, A. S A1 Thompson, Ann A1 Regan, Regina A1 Pilorge, Marion A1 Pellecchia, Giovanna A1 Pagnamenta, Alistair, T A1 Oliveira, Bárbara A1 Marshall, Christian, R A1 Magalhaes, Tiago, R A1 Lowe, Jennifer, K A1 Howe, Jennifer, L A1 Griswold, Anthony, J A1 Gilbert, John A1 Duketis, Eftichia A1 Dombroski, Beth, A A1 de Jonge, Maretha, V A1 Cuccaro, Michael A1 Crawford, Emily, L A1 Correia, Catarina, T A1 Conroy, Judith A1 Conceição, Inês, C A1 Chiocchetti, Andreas, G A1 Casey, Jillian, P A1 Cai, Guiqing A1 Cabrol, Christelle A1 Bolshakova, Nadia A1 Bacchelli, Elena A1 Anney, Richard A1 Gallinger, Steven A1 Cotterchio, Michelle A1 Casey, Graham A1 Zwaigenbaum, Lonnie A1 Wittemeyer, Kerstin A1 Wing, Kirsty A1 Wallace, Simon A1 van Engeland, Herman A1 Tryfon, Ana A1 Thomson, Susanne A1 Soorya, Latha A1 Rogé, Bernadette A1 Roberts, Wendy A1 Poustka, Fritz A1 Mouga, Susana A1 Minshew, Nancy A1 Mcinnes, Alison, L A1 Mcgrew, Susan, G A1 Lord, Catherine A1 Leboyer, Marion A1 Le Couteur, Ann, S A1 Kolevzon, Alexander A1 Jiménez González, Patricia A1 Jacob, Suma A1 Holt, Richard A1 Guter, Stephen A1 Green, Jonathan A1 Green, Andrew A1 Gillberg, Christopher A1 Fernandez, Bridget, A A1 Duque, Frederico A1 Delorme, Richard A1 Dawson, Geraldine A1 Chaste, Pauline A1 Café, Cátia A1 Brennan, Sean A1 Bourgeron, Thomas A1 Bolton, Patrick, F A1 Bölte, Sven A1 Bernier, Raphael A1 Baird, Gillian A1 Bailey, Anthony, J A1 Anagnostou, Evdokia A1 Almeida, Joana A1 Wijsman, Ellen, M A1 Vieland, Veronica, J A1 Vicente, Astrid, M A1 Schellenberg, Gerard, D A1 Pericak-Vance, Margaret A1 Paterson, Andrew, D A1 Parr, Jeremy, R A1 Oliveira, Guiomar A1 Nurnberger, John, I A1 Monaco, Anthony, P A1 Maestrini, Elena A1 Klauck, Sabine, M A1 Hakonarson, Hakon A1 Haines, Jonathan, L A1 Geschwind, Daniel, H A1 Freitag, Christine, M A1 Folstein, Susan, E A1 Ennis, Sean A1 Coon, Hilary A1 Battaglia, Agatino A1 Szatmari, Peter A1 Sutcliffe, James, S A1 Hallmayer, Joachim A1 Gill, Michael A1 Cook, Edwin, H A1 Buxbaum, Joseph, D A1 Devlin, Bernie A1 Gallagher, Louise A1 Betancur, Catalina A1 Scherer, Stephen, W PB HAL CCSD; Elsevier (Cell Press) YR 2014 K1 de novo K1 inherited K1 gene networks K1 pathways K1 Copy Number Variation K1 CHD2 K1 HDAC4 K1 GDI1 K1 autism K1 rare CNV K1 SETD5 K1 [SDV.GEN]Life Sciences [q-bio]/Genetics JF info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2014.03.018 LK http://dx.doi.org/https://inserm.hal.science/inserm-00986225 DO https://inserm.hal.science/inserm-00986225 SF ELIB - SuUB Bremen
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