Authors:
Dechairo, B
Dimon, C
van Heel, D
Mackay, I
Edwards, M
Scambler, P
Jewell, D
Cardon, L
Lench, N
Carey, A
Citation: B. Dechairo et al., Replication and extension studies of inflammatory bowel disease susceptibility regions confirm linkage to chromosome 6p (IBD3), EUR J HUM G, 9(8), 2001, pp. 627-633
Authors:
Deeble, VJ
Roberts, E
Jackson, A
Lench, N
Karban, G
Woods, CG
Citation: Vj. Deeble et al., The continuing failure to recognise Alstrom syndrome and further evidence of genetic homogeneity, J MED GENET, 37(3), 2000, pp. 219-219
Authors:
Toomes, C
James, J
Wood, AJ
Wu, CL
McCormick, D
Lench, N
Hewitt, C
Moynihan, L
Roberts, E
Woods, CG
Markham, A
Wong, M
Widmer, R
Ghaffar, KA
Pemberton, M
Hussein, IR
Temtamy, SA
Davies, R
Read, AP
Sloan, P
Dixon, MJ
Thakker, NS
Citation: C. Toomes et al., Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosis, NAT GENET, 23(4), 1999, pp. 421-424
Authors:
Moynihan, L
Houseman, M
Newton, V
Mueller, R
Lench, N
Citation: L. Moynihan et al., DFNB20: a novel locus for autosomal recessive, non-syndromal sensorineuralhearing loss maps to chromosome 11q25-qter, EUR J HUM G, 7(2), 1999, pp. 243-246