Subcortical laminar heterotopia and lissencephaly in two families: a single X linked dominant gene.

Por Pinard, J M, Motte, J, Chiron, C, Brian, R, Andermann, E, Dulac, O
Publicado em 1994

De novo t(X;21)(q28;q11) in a girl with phenotypic features of Williams-Beuren syndrome.

Por Telvi, L, Pinard, J M, Ion, R, Sinet, P M, Nicole, A, Feingold, J, Dulac, O, Pompidou, A, Ponsot, G
Publicado em 1992

Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22.

Por des Portes, V, Pinard, J M, Smadja, D, Motte, J, Boespflüg-Tanguy, O, Moutard, M L, Desguerre, I, Billuart, P, Carrie, A, Bienvenu, T, Vinet, M C, Bachner, L, Beldjord, C, Dulac, O, Kahn, A, Ponsot, G, Chelly, J
Publicado em 1997