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Current Opinion in Genetics & Development|May 30, 2009
Duplication hotspots, rare genomic disorders, and common diseaseHeather C Mefford, Evan E EichlerCurrent Opinion in Genetics & Development|May 14, 2013
Microdeletion syndromesGemma L Carvill, Heather C MeffordGenome Medicine|August 26, 2015
Advancing epilepsy genetics in the genomic eraCandace T Myers, Heather C MeffordGenome Medicine|October 7, 2010
Genetically complex epilepsies, copy number variants and syndrome constellationsHeather C Mefford, John C MulleyCurrent Opinion in Neurology|January 22, 2011
Genetic contribution to common epilepsiesSanjay M Sisodiya, Heather C MeffordJournal of Pediatric Genetics|September 13, 2016
Next-Generation Sequencing in Intellectual DisabilityGemma L Carvill, Heather C MeffordNature Reviews. Neurology|August 13, 2014
Epilepsy: Beyond the single nucleotide variant in epilepsy geneticsIngrid E Scheffer, Heather C MeffordEpilepsy & Behavior : E&B|June 13, 2013
The unexpected role of copy number variations in juvenile myoclonic epilepsyIngo Helbig, Corinna Hartmann, Heather C MeffordAmerican Journal of Medical Genetics. Part A|October 6, 2018
A de novo in-frame deletion of CASK gene causes early onset infantile spasms and supratentorial cerebral malformation in a female patientXiuhua Bozarth, Kimberly Foss, Heather C MeffordPageof 38