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A novel approach of homozygous haplotype sharing identifies..:
Casey, Jillian P
;
Magalhaes, Tiago
;
Conroy, Judith M
...
qt3k8329tm. , 2012
Link:
https://escholarship.org/uc/item/3k8329tm
RT Journal T1
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt3k8329tm&Exemplar=1&LAN=DE A1 Casey, Jillian P A1 Magalhaes, Tiago A1 Conroy, Judith M A1 Regan, Regina A1 Shah, Naisha A1 Anney, Richard A1 Shields, Denis C A1 Abrahams, Brett S A1 Almeida, Joana A1 Bacchelli, Elena A1 Bailey, Anthony J A1 Baird, Gillian A1 Battaglia, Agatino A1 Berney, Tom A1 Bolshakova, Nadia A1 Bolton, Patrick F A1 Bourgeron, Thomas A1 Brennan, Sean A1 Cali, Phil A1 Correia, Catarina A1 Corsello, Christina A1 Coutanche, Marc A1 Dawson, Geraldine A1 de Jonge, Maretha A1 Delorme, Richard A1 Duketis, Eftichia A1 Duque, Frederico A1 Estes, Annette A1 Farrar, Penny A1 Fernandez, Bridget A A1 Folstein, Susan E A1 Foley, Suzanne A1 Fombonne, Eric A1 Freitag, Christine M A1 Gilbert, John A1 Gillberg, Christopher A1 Glessner, Joseph T A1 Green, Jonathan A1 Guter, Stephen J A1 Hakonarson, Hakon A1 Holt, Richard A1 Hughes, Gillian A1 Hus, Vanessa A1 Igliozzi, Roberta A1 Kim, Cecilia A1 Klauck, Sabine M A1 Kolevzon, Alexander A1 Lamb, Janine A A1 Leboyer, Marion A1 Le Couteur, Ann A1 Leventhal, Bennett L A1 Lord, Catherine A1 Lund, Sabata C A1 Maestrini, Elena A1 Mantoulan, Carine A1 Marshall, Christian R A1 McConachie, Helen A1 McDougle, Christopher J A1 McGrath, Jane A1 McMahon, William M A1 Merikangas, Alison A1 Miller, Judith A1 Minopoli, Fiorella A1 Mirza, Ghazala K A1 Munson, Jeff A1 Nelson, Stanley F A1 Nygren, Gudrun A1 Oliveira, Guiomar A1 Pagnamenta, Alistair T A1 Papanikolaou, Katerina A1 Parr, Jeremy R A1 Parrini, Barbara A1 Pickles, Andrew A1 Pinto, Dalila A1 Piven, Joseph A1 Posey, David J A1 Poustka, Annemarie A1 Poustka, Fritz A1 Ragoussis, Jiannis A1 Roge, Bernadette A1 Rutter, Michael L A1 Sequeira, Ana F A1 Soorya, Latha A1 Sousa, Inês A1 Sykes, Nuala A1 Stoppioni, Vera A1 Tancredi, Raffaella A1 Tauber, Maïté A1 Thompson, Ann P A1 Thomson, Susanne A1 Tsiantis, John A1 Van Engeland, Herman A1 Vincent, John B A1 Volkmar, Fred A1 Vorstman, Jacob AS A1 Wallace, Simon A1 Wang, Kai A1 Wassink, Thomas H A1 White, Kathy A1 Wing, Kirsty PB eScholarship, University of California YR 2012 K1 Autism K1 Genetics K1 Mental Health K1 Intellectual and Developmental Disabilities (IDD) K1 Brain Disorders K1 Biotechnology K1 Pediatric K1 Human Genome K1 Aetiology K1 2.1 Biological and endogenous factors K1 Adult K1 Child K1 Child Development Disorders K1 Pervasive K1 Cluster Analysis K1 Cohort Studies K1 DNA Copy Number Variations K1 Female K1 Genetic Predisposition to Disease K1 Genome-Wide Association Study K1 Genotype K1 Haplotypes K1 Homozygote K1 Humans K1 Linkage Disequilibrium K1 Male K1 Middle Aged K1 Nuclear Family K1 Polymorphism K1 Single Nucleotide K1 Complementary and Alternative Medicine K1 Paediatrics and Reproductive Medicine K1 Genetics & Heredity JF qt3k8329tm LK http://dx.doi.org/https://escholarship.org/uc/item/3k8329tm DO https://escholarship.org/uc/item/3k8329tm SF ELIB - SuUB Bremen
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