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DNA methylation episignature, extension of the clinical features, and comparative epigenomic profiling of Hao-Fountain syndrome caused by variants in USP7 by Laan, Liselot van der (Author) , Karimi, Karim (Author) , Rooney, Kathleen (Author) , Lauffer, Peter (Author) , McConkey, Haley (Author) , Caro, Pilar (Author) , Relator, Raissa (Author) , Levy, Michael A. (Author) , Bhai, Pratibha (Author) , Mignot, Cyril (Author) , Keren, Boris (Author) , Briuglia, Silvana (Author) , Sobering, Andrew K. (Author) , Li, Dong (Author) , Vissers, Lisenka E. L. M. (Author) , Dingemans, Alexander J. M. (Author) , Valenzuela, Irene (Author) , Verberne, Eline A. (Author) , Misra-Isrie, Mala (Author) , Zwijnenburg, Petra J. G. (Author) , Waisfisz, Quinten (Author) , Alders, Mariëlle (Author) , Sailer, Sebastian (Author) , Schaaf, Christian P. (Author) , Mannens, Marcel M. A. M. (Author) , Sadikovic, Bekim (Author) , van Haelst, Mieke M. (Author) , Henneman, Peter (Author) ,

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Distinct phenotypes of shank2 mouse models reflect neuropsychiatric spectrum disorders of human patients with SHANK2 variants by Eltokhi, Ahmed (Author) , Rappold, Gudrun (Author) , Sprengel, Rolf (Author) ,

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Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation by Berkel, Simone (Author) , Marshall, Christian R. (Author) , Weiß, Birgit (Author) , Howe, Jennifer (Author) , Röth, Ralph (Author) , Moog, Ute (Author) , Endris, Volker (Author) , Roberts, Wendy (Author) , Szatmari, Peter (Author) , Pinto, Dalila (Author) , Bonin, Michael (Author) , Riess, Angelika (Author) , Engels, Hartmut (Author) , Sprengel, Rolf (Author) , Scherer, Stephen W. (Author) , Rappold, Gudrun (Author) ,