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Neurodevelopmental risk copy number variants in adults with intellectual disabilities and comorbid psychiatric disorders

Autor: Thygesen, Johan H., Wolfe, Kate, McQuillin, Andrew, Viñas-Jornet, Marina, Baena Díez, Neus, Brison, Nathalie, D'Haenens, Greet, Esteba-Castillo, Susanna, Gabau, Elisabeth, Ribas-Vidal, Núria, Ruiz, Anna, Vermeesch, Joris, Weyts, Eddy, Novell, Ramon, Buggenhout, Griet Van, Strydom, André, Bass, Nicholas, Guitart, Míriam, Vogels, Annick, Universitat Autònoma de Barcelona

Publikováno v: Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
The British Journal of Psychiatry
Thygesen, J H, Wolfe, K, Mcquillin, A, Viñas-jornet, M, Baena, N, Brison, N, D'haenens, G, Esteba-castillo, S, Gabau, E, Ribas-vidal, N, Ruiz, A, Vermeesch, J, Weyts, E, Novell, R, Buggenhout, G V, Strydom, A, Bass, N, Guitart, M & Vogels, A 2018, ' Neurodevelopmental risk copy number variants in adults with intellectual disabilities and comorbid psychiatric disorders ', British Journal of Psychiatry, vol. 212, no. 5, pp. 287-294 . https://doi.org/10.1192/bjp.2017.65

BackgroundCopy number variants (CNVs) are established risk factors for neurodevelopmental disorders. To date the study of CNVs in psychiatric illness has focused on single disorder populations. The role of CNVs in individuals with intellectual disabi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::982a262f2b96d97559e1406bc3760c5e
https://ddd.uab.cat/record/227912

MECP2 mutations are an infrequent cause of mental retardation associated with neurological problems in male patients

Autor: Moog, Ute^1,2 ute.moog@gen.unimaas.nl, Roozendaal, Kees Van¹, Smeets, Eric^1,3, Tserpelis, Demis¹, Devriendt, Koen³, Buggenhout, Griet Van³, Frijns, Jean-Pierre^1,3, Schrander-Stumpel, Connie^1,2

Publikováno v: Brain & Development. Jun2006, Vol. 28 Issue 5, p305-310. 6p.