Showing 1 - 3 results of 3 for search 'Represa, A', query time: 0.34s
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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
Published 2017Journal article -
2
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
Published 2013Journal article -
3
Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria. by Jaglin, X, Poirier, K, Saillour, Y, Buhler, E, Tian, G, Bahi-Buisson, N, Fallet-Bianco, C, Phan-Dinh-Tuy, F, Kong, X, Bomont, P, Castelnau-Ptakhine, L, Odent, S, Loget, P, Kossorotoff, M, Snoeck, I, Plessis, G, Parent, P, Beldjord, C, Cardoso, C, Represa, A, Flint, J, Keays, D, Cowan, N, Chelly, J
Published 2009Journal article