Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndromeTiong Yang Tan, Gregory B. Peters, Anne Ronan et al.|Journal of Medical Genetics|2009Cited by 135
Loss of symmetric cell division of apical neural progenitors drives DENND5A-related developmental and epileptic encephalopathyEmily Banks, Hane Lee, Huda G. El Said et al.|Nature Communications|2024Cited by 5