| 1 | DEL9Q21 |
| A novel microdeletion syndrome at 9q21.13 characterised by mental retardation, speech delay, epilepsy and characteristic facial features. | |
| Boudry-Labis E, Demeer B, Le Caignec C, Isidor B, Mathieu-Dramard M, Plessis G, George AM, Taylor J, Aftimos S, Wiemer-Kruel A, Kohlhase J, Annerén G, Firth H, Simonic I, Vermeesch J, Thuresson AC, Copin H, Love DR, Andrieux J. | |
| Eur J Med Genet 56(3):163-70. doi: 10.1016/j.ejmg.2012.12.006. Epub 2012 Dec 29. 2013 | |