Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability. by Pagnamenta, A, Khan, H, Walker, S, Gerrelli, D, Wing, K, Bonaglia, M, Giorda, R, Berney, T, Mani, E, Molteni, M, Pinto, D, Le Couteur, A, Hallmayer, J, Sutcliffe, J, Szatmari, P, Paterson, A, Scherer, S, Vieland, V, Monaco, A

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability by Pagnamenta, A, Khan, H, Walker, S, Gerrelli, D, Wing, K, Bonaglia, M, Giorda, R, Berney, T, Mani, E, Molteni, M, Pinto, D, Le Couteur, A, Hallmayer, J, Sutcliffe, J, Szatmari, P, Paterson, A, Scherer, S, Vieland, V, Monaco, A

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures. by Sharp, A, Mefford, H, Li, K, Baker, C, Skinner, C, Stevenson, R, Schroer, R, Novara, F, De Gregori, M, Ciccone, R, Broomer, A, Casuga, I, Wang, Y, Xiao, C, Barbacioru, C, Gimelli, G, Bernardina, B, Torniero, C, Giorda, R, Regan, R, Murday, V, Mansour, S, Fichera, M, Castiglia, L, Failla, P