KANSL1 gene disruption associated with the full clinical spectrum of 17q21.31 microdeletion syndrome. - Moreno-Igoa, María; Hernández-Charro, Blanca; Bengoa-Alonso, Amaya; Pérez-Juana-del-Casal, Aranzazu; Romero-Ibarra, Carlos; Nieva-Echebarria, Beatriz; Ramos-Arroyo, María Antonia (BMC Medical Genetics, 2015)