SENSORIMOTOR GATING AND SOCIAL BEHAVIOUR IN GTF2IRD1 KNOCKOUT MOUSE by Schneider, T, Rawlins, J, Tassabehji, M

Screening for subtelomeric chromosome deletions in children with idiopathic mental retardation by Slavotinek, A, Knight, S, Tassabehji, M, ClaytonSmith, J, Kingston, H, Gaunt, L, Flint, J, Donnai, D

Anxious, hypoactive phenotype combined with motor deficits in Gtf2ird1 null mouse model relevant to Williams syndrome. by Schneider, T, Skitt, Z, Liu, Y, Deacon, R, Flint, J, Karmiloff-Smith, A, Rawlins, J, Tassabehji, M

Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin. by Hennies, H, Kornak, U, Zhang, H, Egerer, J, Zhang, X, Seifert, W, Kühnisch, J, Budde, B, Nätebus, M, Brancati, F, Wilcox, W, Müller, D, Kaplan, P, Rajab, A, Zampino, G, Fodale, V, Dallapiccola, B, Newman, W, Metcalfe, K, Clayton-Smith, J, Tassabehji, M, Steinmann, B, Barr, F, Nürnberg, P, Wieacker, P