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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
Published 2011Journal article -
2
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
Published 2011Journal article -
3
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
Published 2008Journal article