1. A survey of seizures and current treatments in 15q duplication syndrome. Issue 3 (6th February 2014) Authors: Conant, Kerry D.; Finucane, Brenda; Cleary, Nicole; Martin, Ashley; Muss, Candace; Delany, Mary; Murphy, Erin K.; Rabe, Olivia; Luchsinger, Kadi; Spence, Sarah J.; Schanen, Carolyn; Devinsky, Orrin; Cook, Edwin H.; LaSalle, Janine; Reiter, Lawrence T.; Thibert, Ronald L. Journal: Epilepsia Issue: Volume 55:Issue 3(2014:Mar.) Page Start: 396 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in rett syndrome. Issue 7 (21st May 2013) Authors: Chapleau, Christopher A.; Lane, Jane; Kirwin, Susan M.; Schanen, Carolyn; Vinette, Kathy M.B.; Stubbolo, Danielle; MacLeod, Patrick; Percy, Alan K. Journal: American journal of medical genetics Issue: Volume 161:Issue 7(2013:Jul.) Page Start: 1638 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Erratum to "Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndrome", Am J Med Genet Part A 161A:1638–1646. Issue 5 (May 2014) Authors: Chapleau, Christopher A.; Lane, Jane; Kirwin, Susan; Schanen, Carolyn; Vinette, Kathy M. B.; Stubbolo, Danielle; MacLeod, Patrick; Glaze, Daniel G.; Motil, Kathleen J.; Neul, Jeffrey L.; Skinner, Steven A.; Kaufmann, Walter E.; Percy, Alan K. Journal: American journal of medical genetics Issue: Volume 164:Issue 5(2014.) Page Start: 1346 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗