Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome. - Willemsen, Marjolein H.; Fernandez, Bridget A.; Bacino, Carlos A.; Gerkes, Erica; de Brouwer, Arjan P. M.; Pfundt, Rolph; Sikkema-Raddatz, Birgit; Scherer, Stephen W.; Marshall, Christian R.; Potocki, Lorraine; van Bokhoven, Hans; Kleefstra, Tjitske (European Journal of Human Genetics, 2010)