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Results: 1-5 |
Results: 5

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: Kindelan, SA Brook, AH Gangemi, L Lench, N Wong, FSL Fearne, J Jackson, Z Foster, G Stringer, BMJ
Citation: Sa. Kindelan et al., Detection of a novel mutation in X-linked amelogenesis imperfecta, J DENT RES, 79(12), 2000, pp. 1978-1982

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
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