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Human molecular genetics, ISSN 0964-6906, 2009, Volume 18, Issue 5, pp. 988 - 996
Journal Article
European journal of human genetics : EJHG, ISSN 1018-4813, 08/2010, Volume 18, Issue 8, pp. 902 - 908
Journal Article
by Gudbjartsson, Daniel F and Bjornsdottir, Unnur S and Halapi, Eva and Helgadottir, Anna and Sulem, Patrick and Jonsdottir, Gudrun M and Thorleifsson, Gudmar and Helgadottir, Hafdis and Steinthorsdottir, Valgerdur and Stefansson, Hreinn and Williams, Carolyn and Hui, Jennie and Beilby, John and Warrington, Nicole M and James, Alan and Palmer, Lyle J and Koppelman, Gerard H and Heinzmann, Andrea and Krueger, Marcus and Boezen, H Marike and Wheatley, Amanda and Altmuller, Janine and Shin, Hyoung Doo and Uh, Soo-Taek and Cheong, Hyun Sub and Jonsdottir, Brynja and Gislason, David and Park, Choon-Sik and Rasmussen, Linda M and Porsbjerg, Celeste and Hansen, Jakob W and Backer, Vibeke and Werge, Thomas and Janson, Christer and Jönsson, Ulla-Britt and Ng, Maggie C Y and Chan, Juliana and So, Wing Yee and Ma, Ronald and Shah, Svati H and Granger, Christopher B and Quyyumi, Arshed A and Levey, Allan I and Vaccarino, Viola and Reilly, Muredach P and Rader, Daniel J and Williams, Michael J A and van Rij, Andre M and Jones, Gregory T and Trabetti, Elisabetta and Malerba, Giovanni and Pignatti, Pier Franco and Boner, Attilio and Pescollderungg, Lydia and Girelli, Domenico and Olivieri, Oliviero and Martinelli, Nicola and Ludviksson, Bjorn R and Ludviksdottir, Dora and Eyjolfsson, Gudmundur I and Arnar, David and Thorgeirsson, Gudmundur and Deichmann, Klaus and Thompson, Philip J and Wjst, Matthias and Hall, Ian P and Postma, Dirkje S and Gislason, Thorarinn and Gulcher, Jeffrey and Kong, Augustine and Jonsdottir, Ingileif and Thorsteinsdottir, Unnur and Stefansson, Kari
Nature genetics, ISSN 1546-1718, 2009, Volume 41, Issue 3, pp. 342 - 347
Journal Article
Human molecular genetics, ISSN 0964-6906, 03/2009, Volume 18, Issue 5, pp. 988 - 996
Deletions within the neurexin 1 gene (NRXN1; 2p16.3) are associated with autism and have also been reported in two families with schizophrenia. We examined... 
MICRODELETION | POPULATION | HUMAN GENOME | STRUCTURAL VARIANTS | AUTISM SPECTRUM DISORDER | RISK | REARRANGEMENTS | ADVANCING PATERNAL AGE | UMCG Approved | CARDIO-FACIAL SYNDROME | COPY-NUMBER VARIATION
Journal Article
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