KANSL1 gene disruption associated with the full clinical spectrum of 17q21.31 microdeletion syndrome

por Moreno-Igoa, María, Hernández-Charro, Blanca, Bengoa-Alonso, Amaya, Pérez-Juana-del-Casal, Aranzazu, Romero-Ibarra, Carlos, Nieva-Echebarria, Beatriz, Ramos-Arroyo, María Antonia
Publicado 2015