Torthaí cuardaigh - Nygren Gudrun

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  1. 1
    Íomhá chlúdaigh

    Mutation analysis of the <it>NSD1 </it>gene in patients with autism spectrum disorders and macrocephaly de réir 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

    Foilsithe / Cruthaithe 2007
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  2. 2
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    Mutation screening of <it>NOS1AP </it>gene in a large sample of psychiatric patients and controls de réir 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

    Foilsithe / Cruthaithe 2010
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  3. 3
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    An investigation of ribosomal protein L10 gene in autism spectrum disorders de réir 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

    Foilsithe / Cruthaithe 2009
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