Modelling human microdeletion syndromes by chromosome engineering in mice by Shaw-Smith, C, Storer, M, Szumska, D, Scambler, P, Bhattacharya, S, Bradley, A

Analysis of the epsilon-sarcoglycan gene in familial and sporadic myoclonus-dystonia: evidence for genetic heterogeneity. by Valente, E, Misbahuddin, A, Brancati, F, Placzek, MR, Garavaglia, B, Salvi, S, Nemeth, A, Shaw-Smith, C, Nardocci, N, Bentivoglio, A, Berardelli, A, Eleopra, R, Dallapiccola, B, Warner, T

VACTERL/caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5. by Szumska, D, Pieles, G, Essalmani, R, Bilski, M, Mesnard, D, Kaur, K, Franklyn, A, El Omari, K, Jefferis, J, Bentham, J, Taylor, J, Schneider, J, Arnold, S, Johnson, P, Tymowska-Lalanne, Z, Stammers, D, Clarke, K, Neubauer, S, Morris, A, Brown, S, Shaw-Smith, C, Cama, A, Capra, V, Ragoussis, J, Constam, D

Development, behaviour and sensory processing in Marshall-Smith syndrome and Malan syndrome: phenotype comparison in two related syndromes by Mulder, PA, van Balkom, IDC, Landlust, AM, Priolo, M, Menke, LA, Acero, IH, Alkuraya, FS, Arias, P, Bernardini, L, Bijlsma, EK, Cole, T, Coubes, C, Dapia, I, Davies, S, Di Donato, N, Elcioglu, NH, Fahrner, JA, Foster, A, González, NG, Huber, I, Iascone, M, Kaiser, A-S, Kamath, A, Kooblall, KG, Lapunzina, P, Liebelt, J, Lynch, SA, Maas, SM, Mammì, C, Mathijssen, IB, McKee, S, Mirzaa, GM, Montgomery, T, Neubauer, D, Neumann, TE, Pintomalli, L, Pisanti, MA, Plomp, AS, Price, S, Salter, C, Santos-Simarro, F, Sarda, P, Schanze, D, Segovia, M, Shaw-Smith, C, Smithson, S, Suri, M, Tatton-Brown, K, Tenorio, J, Thakker, RV