Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Intellectual Disability and DLG2[original query] |
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Clinical significance of de novo and inherited copy-number variation. Human mutation 2013 Dec 34 (12): 1679-87. Vulto-van Silfhout Anneke T, Hehir-Kwa Jayne Y, van Bon Bregje W M, Schuurs-Hoeijmakers Janneke H M, Meader Stephen, Hellebrekers Claudia J M, Thoonen Ilse J M, de Brouwer Arjan P M, Brunner Han G, Webber Caleb, Pfundt Rolph, de Leeuw Nicole, de Vries Bert B |
Behavioural and molecular characterisation of the Dlg2 haploinsufficiency rat model of genetic risk for psychiatric disorder. Genes, brain, and behavior 2022 Jan e12797. Waldron Sophie, Pass Rachel, Griesius Simonas, Mellor Jack R, Robinson Emma S J, Thomas Kerrie L, Wilkinson Lawrence S, Humby Trevor, Hall Jeremy, Dwyer Dominic |
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- Page last updated:May 06, 2024
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