Structural insights into the p97-Ufd1-Npl4 complex. od Pye, V, Beuron, F, Keetch, C, McKeown, C, Robinson, C, Meyer, H, Zhang, X, Freemont, P

Inherited neuromuscular junction disorders: Genotype phenotype correlations od Vogt, J, Morgan, N, Harrison, B, Rehal, P, Brueton, L, McKeown, C, Oley, C, Beeson, D, MacDonald, F, Maher, E

Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients. od Wang, Z, Churchman, M, Avizienyte, E, McKeown, C, Davies, S, Evans, D, Ferguson, A, Ellis, I, Xu, W, Yan, Z, Aaltonen, L, Tomlinson, I

Clinical studies on submicroscopic subtelomeric rearrangements: a checklist. od de Vries, B, White, S, Knight, S, Regan, R, Homfray, T, Young, I, Super, M, McKeown, C, Splitt, M, Quarrell, O, Trainer, A, Niermeijer, M, Malcolm, S, Flint, J, Hurst, J, Winter, R

Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3. od Olschwang, S, Markie, D, Seal, S, Neale, K, Phillips, R, Cottrell, S, Ellis, I, Hodgson, S, Zauber, P, Spigelman, A, Iwama, T, Loff, S, McKeown, C, Marchese, C, Sampson, J, Davies, S, Talbot, I, Wyke, J, Thomas, G, Bodmer, W, Hemminki, A, Avizienyte, E, de la Chapelle, A, Aaltonen, L, Tomlinson, I