A novel strategy combining array-CGH, whole-exome sequencing and in utero electroporation in rodents to identify causative genes for brain malformations by Conti, V, Carabalona, A, Pallesi-Pocachard, E, Leventer, R, Schaller, F, Parrini, E, Deparis, A, Watrin, F, Buhler, E, Novara, F, Lise, S, Pagnamenta, A, Kini, U, Taylor, J, Zuffardi, O, Represa, A, Keays, D, Guerrini, R, Falace, A, Cardoso, C

Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene. by Conti, V, Carabalona, A, Pallesi-Pocachard, E, Parrini, E, Leventer, R, Buhler, E, McGillivray, G, Michel, F, Striano, P, Mei, D, Watrin, F, Lise, S, Pagnamenta, A, Taylor, J, Kini, U, Clayton-Smith, J, Novara, F, Zuffardi, O, Dobyns, W, Scheffer, I, Robertson, S, Berkovic, S, Represa, A, Keays, D, Cardoso, C