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Results: 1-9 |
Results: 9

Authors: Mitchell, BD Gibbons, B Allen, LR Stella, J D'Mello, SR
Citation: Bd. Mitchell et al., Aberrant apoptosis in the neurological mutant Flathead is associated with defective cytokinesis of neural progenitor cells, DEV BRAIN R, 130(1), 2001, pp. 53-63

Authors: Gibbons, B
Citation: B. Gibbons, Patents not the problem, TECHNOL REV, 104(5), 2001, pp. 16-16

Authors: Harrison, CJ Gibbons, B Yang, FT Butler, T Cheung, KL Kearney, L Dirscherl, L Bray-Ward, P Gregson, M Ferguson-Smith, M
Citation: Cj. Harrison et al., Multiplex fluorescence in situ hybridization and cross species color banding of a case of chronic myeloid leukemia in blastic crisis with a complex Philadelphia translocation, CANC GENET, 116(2), 2000, pp. 105-110

Authors: Sidwell, RU Pinson, MP Gibbons, B Byatt, SA Svennevik, EC Hastings, RJ Flynn, DM
Citation: Ru. Sidwell et al., Pure trisomy 20p resulting from isochromosome formation and whole arm translocation, J MED GENET, 37(6), 2000, pp. 454-458

Authors: Cockwell, AE Gibbons, B Moore, IE Crolla, JA
Citation: Ae. Cockwell et al., An analphoid supernumerary marker chromosome derived from chromosome 3 ascertained in a fetus with multiple malformations, J MED GENET, 37(10), 2000, pp. 807-809

Authors: Gibbons, B Tan, S Yu, CCW Cheah, E Tan, HL
Citation: B. Gibbons et al., Risk of gonadoblastoma in female patients with Y chromosome abnormalities and dysgenetic gonads, J PAEDIAT C, 35(2), 1999, pp. 210-213

Authors: Gregory, H Gibbons, B Haites, N
Citation: H. Gregory et al., Audit of women attending the Aberdeen Genetic Clinic with a family historyof breast cancer who subsequently develop cancer, DIS MARKER, 15(1-3), 1999, pp. 201-203

Authors: Gibbons, B Tan, SY Kee, SK Quaife, R Lim, ST
Citation: B. Gibbons et al., Interstitial deletion of chromosome 5 in a neonate due to maternal insertion, ins(8;5) (p23;q33q35), AM J MED G, 86(3), 1999, pp. 289-293

Authors: Gibbons, B Tan, SY Barber, JCK Ng, CF Knight, LA Lam, S Ng, I
Citation: B. Gibbons et al., Duplication of 8p with minimal phenotypic effect transmitted from a motherto her two daughters, J MED GENET, 36(5), 1999, pp. 419-422
Risultati: 1-9 |