Whole genome sequencing identifies a de novo 2.1 Mb balanced paracentric inversion disrupting FOXP1 and leading to severe intellectual disability. - Vuillaume, M.-L.; Jeanne, M.; Laumonnier, F.; Toutain, A.; Ung, D.-C.; Quinquis, D.; Besnard, T.; Cogné, B.; Bézieau, S.; Redon, R.; Boland, A.; Deleuze, J.-F. (Clinica Chimica Acta, 2018)