Mutation analysis of the <it>NSD1 </it>gene in patients with autism spectrum disorders and macrocephaly by Delorme Richard, Chaste Pauline, Nygren Gudrun, Cai Guiqing, Buxbaum Joseph D, Goldsmith Juliet, Råstam Maria, Silverman Jeremy M, Hollander Eric, Gillberg Christopher, Leboyer Marion, Betancur Catalina

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Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder by Grabe Hans, Mössner Rainald, Chaste Pauline, Maier Wolfgang, Gennetier Aurélie, Moreno-, Delorme Richard, Ruhrmann Stephan, Falkai Peter, Mouren Marie-Christine, Leboyer Marion, Wagner Michael, Betancur Catalina

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Mutation screening of <it>NOS1AP </it>gene in a large sample of psychiatric patients and controls by Nygren Gudrun, Schuroff Franck, Jamain Stéphane, Chaste Pauline, Anckarsäter Henrik, Scheid Isabelle, Betancur Catalina, Delorme Richard, Herbrecht Evelyn, Dumaine Anne, Mouren Marie, Råstam Maria, Leboyer Marion, Gillberg Christopher, Bourgeron Thomas

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An investigation of ribosomal protein L10 gene in autism spectrum disorders by Rastam Maria, Anckarsäter Henrik, Nygren Gudrun, Goubran-Botros Hany, Betancur Catalina, Chaste Pauline, Durand Christelle M, Fauchereau Fabien, Delorme Richard, Gong Xiaohong, Gillberg I Carina, Kopp Svenny, Mouren-Simeoni, Gillberg Christopher, Leboyer Marion, Bourgeron Thomas

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Mutation screening of <it>ASMT</it>, the last enzyme of the melatonin pathway, in a large sample of patients with Intellectual Disability by Tzschach Andreas, Launay Jean-Marie, Delorme Richard, Van Esch Hilde, de Brouwer Arjan, Moreno Sarah, Jamain Stéphane, Dumaine Anne, Poirier Karine, Botros Hany, Pagan Cecile, Kalscheuer Vera, Lacombe Didier, Briault Sylvain, Laumonnier Frédéric, Raynaud Martine, van Bon Bregje W, Willemsen Marjolein H, Leboyer Marion, Chelly Jamel, Bourgeron Thomas

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