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7. Investigating the genetic basis of fever-associated syndromic epilepsies using copy number variation analysis. Hartmann C; von Spiczak S; Suls A; Weckhuysen S; Buyse G; Vilain C; Van Bogaert P; De Jonghe P; Cook J; Muhle H; Stephani U; Helbig I; Mefford HC Epilepsia; 2015 Mar; 56(3):e26-32. PubMed ID: 25690317 [TBL] [Abstract][Full Text] [Related]
8. Genetic contribution to common epilepsies. Sisodiya SM; Mefford HC Curr Opin Neurol; 2011 Apr; 24(2):140-5. PubMed ID: 21252662 [TBL] [Abstract][Full Text] [Related]
9. Copy number variants in absence epilepsy: Further complications of the picture. Depondt C Neurol Genet; 2016 Apr; 2(2):e67. PubMed ID: 27123485 [TBL] [Abstract][Full Text] [Related]
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11. Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects. Niestroj LM; Perez-Palma E; Howrigan DP; Zhou Y; Cheng F; Saarentaus E; Nürnberg P; Stevelink R; Daly MJ; Palotie A; Lal D; Brain; 2020 Jul; 143(7):2106-2118. PubMed ID: 32568404 [TBL] [Abstract][Full Text] [Related]
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17. Penetrance for copy number variants associated with schizophrenia. Vassos E; Collier DA; Holden S; Patch C; Rujescu D; St Clair D; Lewis CM Hum Mol Genet; 2010 Sep; 19(17):3477-81. PubMed ID: 20587603 [TBL] [Abstract][Full Text] [Related]
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