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American Journal of Human Genetics|October 10, 2007
Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsyHeather C Mefford, Severine Clauin, Andrew J Sharp, et al.American Journal of Medical Genetics. Part A|June 19, 2015
A homozygous B3GAT3 mutation causes a severe syndrome with multiple fractures, expanding the phenotype of linkeropathy syndromesKelly L Jones, Ulrike Schwarze, Margaret P Adam, et al.The Journal of Craniofacial Surgery|January 26, 2013
Regression modeling to inform cell incorporation into therapies for craniosynostosisJames Cray, Gregory M CooperCurrent Opinion in Genetics & Development|November 26, 2003
Genomic regulatory regions: insights from comparative sequence analysisGregory M Cooper, Arend SidowNature Reviews. Genetics|August 19, 2011
Needles in stacks of needles: finding disease-causal variants in a wealth of genomic dataGregory M Cooper, Jay ShendureEpilepsia Open|March 8, 2021
Developmental and epileptic encephalopathy: Personal utility of a genetic diagnosis for familiesJennifer S Jeffrey, Janet Leathem, Chontelle King, et al.Therapeutic Advances in Rare Disease|October 11, 2024
A roadmap to cure CHD2-related disordersStephanie Prince, Emily Bonkowski, Christopher McGraw, et al.Genome Research|February 5, 2008
Qualifying the relationship between sequence conservation and molecular functionGregory M Cooper, Christopher D BrownJournal of Forensic Nursing|November 1, 2006
Interviewing the incarcerated offender convicted of sexually assaulting the elderlyGregory M Cooper, Michael R KingSeizure|October 16, 2018
Dravet syndrome in South African infants: Tools for an early diagnosisAlina I Esterhuizen, Heather C Mefford, Rajkumar S Ramesar, et al.Pageof 38