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2. Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample. Ludwig KU; Schumacher J; Schulte-Körne G; König IR; Warnke A; Plume E; Anthoni H; Peyrard-Janvid M; Meng H; Ziegler A; Remschmidt H; Kere J; Gruen JR; Müller-Myhsok B; Nöthen MM; Hoffmann P Psychiatr Genet; 2008 Dec; 18(6):310-2. PubMed ID: 19018237 [TBL] [Abstract][Full Text] [Related]
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11. Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability. Cope N; Eicher JD; Meng H; Gibson CJ; Hager K; Lacadie C; Fulbright RK; Constable RT; Page GP; Gruen JR Neuroimage; 2012 Oct; 63(1):148-56. PubMed ID: 22750057 [TBL] [Abstract][Full Text] [Related]
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13. Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. Harold D; Paracchini S; Scerri T; Dennis M; Cope N; Hill G; Moskvina V; Walter J; Richardson AJ; Owen MJ; Stein JF; Green ED; O'Donovan MC; Williams J; Monaco AP Mol Psychiatry; 2006 Dec; 11(12):1085-91, 1061. PubMed ID: 17033633 [TBL] [Abstract][Full Text] [Related]
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20. The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domains. Eicher JD; Stein CM; Deng F; Ciesla AA; Powers NR; Boada R; Smith SD; Pennington BF; Iyengar SK; Lewis BA; Gruen JR Genes Brain Behav; 2015 Apr; 14(4):377-85. PubMed ID: 25778907 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]