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A genome-wide scan for common alleles affecting risk for au..:
Anney, Richard
;
Klei, Lambertus
;
Pinto, Dalila
...
info:eu-repo/semantics/altIdentifier/doi/10.1093/hmg/ddq307. , 2010
Link:
https://inserm.hal.science/inserm-00521391
RT Journal T1
A genome-wide scan for common alleles affecting risk for autism
UL https://suche.suub.uni-bremen.de/peid=base-ftinserm:oai:HAL:inserm-00521391v1&Exemplar=1&LAN=DE A1 Anney, Richard A1 Klei, Lambertus A1 Pinto, Dalila A1 Regan, Regina A1 Conroy, Judith A1 Magalhaes, Tiago, R A1 Correia, Catarina A1 Abrahams, Brett, S A1 Sykes, Nuala A1 Pagnamenta, Alistair, T A1 Almeida, Joana A1 Bacchelli, Elena A1 Bailey, Anthony, J A1 Baird, Gillian A1 Battaglia, Agatino A1 Berney, Tom A1 Bolshakova, Nadia A1 Bölte, Sven A1 Bolton, Patrick, F A1 Bourgeron, Thomas A1 Brennan, Sean A1 Brian, Jessica A1 Carson, Andrew, R A1 Casallo, Guillermo A1 Casey, Jillian A1 Chu, Su, H A1 Cochrane, Lynne A1 Corsello, Christina A1 Crawford, Emily, L A1 Crossett, Andrew A1 Dawson, Geraldine A1 de Jonge, Maretha A1 Delorme, Richard A1 Drmic, Irene A1 Duketis, Eftichia A1 Duque, Frederico A1 Estes, Annette A1 Farrar, Penny A1 Fernandez, Bridget, A A1 Folstein, Susan, E A1 Fombonne, Eric A1 Freitag, Christine, M A1 Gilbert, John A1 Gillberg, Christopher A1 Glessner, Joseph, T A1 Goldberg, Jeremy A1 Green, Jonathan A1 Guter, Stephen, J A1 Hakonarson, Hakon A1 Heron, Elizabeth, A A1 Hill, Matthew A1 Holt, Richard A1 Howe, Jennifer, L A1 Hughes, Gillian A1 Hus, Vanessa A1 Igliozzi, Roberta A1 Kim, Cecilia A1 Klauck, Sabine, M A1 Kolevzon, Alexander A1 Korvatska, Olena A1 Kustanovich, Vlad A1 Lajonchere, Clara, M A1 Lamb, Janine, A A1 Laskawiec, Magdalena A1 Leboyer, Marion A1 Le Couteur, Ann A1 Leventhal, Bennett, L A1 Lionel, Anath, C A1 Liu, Xiao-Qing A1 Lord, Catherine A1 Lotspeich, Linda A1 Lund, Sabata, C A1 Maestrini, Elena A1 Mahoney, William A1 Mantoulan, Carine A1 Marshall, Christian, R A1 Mcconachie, Helen A1 Mcdougle, Christopher, J A1 Mcgrath, Jane A1 Mcmahon, William, M A1 Melhem, Nadine, M A1 Merikangas, Alison A1 Migita, Ohsuke A1 Minshew, Nancy, J A1 Mirza, Ghazala, K A1 Munson, Jeff A1 Nelson, Stanley, F A1 Noakes, Carolyn A1 Noor, Abdul A1 Nygren, Gudrun A1 Oliveira, Guiomar A1 Papanikolaou, Katerina A1 Parr, Jeremy, R A1 Parrini, Barbara A1 Paton, Tara A1 Pickles, Andrew A1 Piven, Joseph A1 Posey, David, J A1 Poustka, Annemarie A1 Poustka, Fritz A1 Prasad, Aparna A1 Ragoussis, Jiannis A1 Renshaw, Katy A1 Rickaby, Jessica A1 Roberts, Wendy A1 Roeder, Kathryn A1 Roge, Bernadette A1 Rutter, Michael, L A1 Bierut, Laura, J A1 Rice, John, P A1 Salt, Jeff A1 Sansom, Katherine A1 Sato, Daisuke A1 Segurado, Ricardo A1 Senman, Lili A1 Shah, Naisha A1 Sheffield, Val, C A1 Soorya, Latha A1 Sousa, Inês A1 Stoppioni, Vera A1 Strawbridge, Christina A1 Tancredi, Raffaella A1 Tansey, Katherine A1 Thiruvahindrapduram, Bhooma A1 Thompson, Ann, P A1 Thomson, Susanne A1 Tryfon, Ana A1 Tsiantis, John A1 van Engeland, Herman A1 Vincent, John, B A1 Volkmar, Fred A1 Wallace, Simon A1 Wang, Kai A1 Wang, Zhouzhi A1 Wassink, Thomas, H A1 Wing, Kirsty A1 Wittemeyer, Kerstin A1 Wood, Shawn A1 Yaspan, Brian, L A1 Zurawiecki, Danielle, M A1 Zwaigenbaum, Lonnie A1 Betancur, Catalina A1 Buxbaum, Joseph, D A1 Cantor, Rita, M A1 Cook, Edwin, H A1 Coon, Hilary A1 Cuccaro, Michael, L A1 Gallagher, Louise A1 Geschwind, Daniel, H A1 Gill, Michael A1 Haines, Jonathan, L A1 Miller, Judith A1 Monaco, Anthony, P A1 Nurnberger, John, I A1 Paterson, Andrew, D A1 Pericak-Vance, Margaret, A A1 Schellenberg, Gerard, D A1 Scherer, Stephen, W A1 Sutcliffe, James, S A1 Szatmari, Peter A1 Vicente, Astrid, M A1 Vieland, Veronica, J A1 Wijsman, Ellen, M A1 Devlin, Bernie A1 Ennis, Sean A1 Hallmayer, Joachim PB HAL CCSD; Oxford University Press (OUP) YR 2010 K1 MESH: Alleles K1 MESH: Autistic Disorder K1 MESH: Humans K1 MESH: Polymorphism K1 Single Nucleotide K1 MESH: Risk Factors K1 MESH: DNA Copy Number Variations K1 MESH: Databases K1 Genetic K1 MESH: European Continental Ancestry Group K1 MESH: Genetic Predisposition to Disease K1 MESH: Genetic Variation K1 MESH: Genome K1 Human K1 MESH: Genome-Wide Association Study K1 MESH: Genotype K1 [SDV.GEN]Life Sciences [q-bio]/Genetics JF info:eu-repo/semantics/altIdentifier/doi/10.1093/hmg/ddq307 LK http://dx.doi.org/https://inserm.hal.science/inserm-00521391 DO https://inserm.hal.science/inserm-00521391 SF ELIB - SuUB Bremen
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