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Neurology. Genetics|July 15, 2025
The Association Between Sleep Phenotypes and Epilepsy GenesJonathan Read Gaillard, Gita Gupta, Heather C Mefford, et al.Annual Review of Genomics and Human Genetics|August 30, 2005
Trade-offs in detecting evolutionarily constrained sequence by comparative genomicsEric A Stone, Gregory M Cooper, Arend SidowAmerican Journal of Medical Genetics. Part A|May 21, 2013
Deletions of 16p11.2 and 19p13.2 in a family with intellectual disability and generalized epilepsyAlexander G Bassuk, Eileen Geraghty, Shu Wu, et al.Epilepsia|November 5, 2011
Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndromeHiltrud Muhle, Heather C Mefford, Tanja Obermeier, et al.Epilepsy Research|November 20, 2013
Iterative phenotyping of 15q11.2, 15q13.3 and 16p13.11 microdeletion carriers in pediatric epilepsiesJohanna A Jähn, Sarah von Spiczak, Hiltrud Muhle, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 14, 2020
Levetiracetam efficacy in PCDH19 Girls Clustering EpilepsyLynette G Sadleir, Kristy L Kolc, Chontelle King, et al.Molecular Autism|October 17, 2017
Clinical phenotype of ASD-associated DYRK1A haploinsufficiencyRachel K Earl, Tychele N Turner, Heather C Mefford, et al.American Journal of Medical Genetics. Part A|October 14, 2016
Description of a new oncogenic mechanism for atypical teratoid rhabdoid tumors in patients with ring chromosome 22Heather M Byers, Margaret P Adam, Amy LaCroix, et al.BMC Bioinformatics|December 14, 2004
ABC: software for interactive browsing of genomic multiple sequence alignment dataGregory M Cooper, Senthil A G Singaravelu, Arend SidowNature Genetics|September 5, 2007
Mutational and selective effects on copy-number variants in the human genomeGregory M Cooper, Deborah A Nickerson, Evan E EichlerPageof 38