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Results: 1-6 |
Results: 6

Authors: Cardno, AG Holmans, PA Rees, MI Jones, LA McCarthy, GM Hamshere, ML Williams, NM Norton, N Williams, HJ Fenton, I Murphy, KC Sanders, RD Gray, MY O'Donovan, MC McGuffin, P Owen, MJ
Citation: Ag. Cardno et al., A genomewide linkage study of age at onset in schizophrenia, AM J MED G, 105(5), 2001, pp. 439-445

Authors: Krawczak, M Ball, EV Fenton, I Stenson, PD Abeysinghe, S Thomas, N Cooper, DN
Citation: M. Krawczak et al., Human gene mutation database - A biomedical information and research resource, HUM MUTAT, 15(1), 2000, pp. 45-51

Authors: Rees, MI Watts, P Fenton, I Clarke, A Snell, RG Owen, MJ Gray, J
Citation: Mi. Rees et al., Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA(3)), HUM GENET, 106(2), 2000, pp. 206-209

Authors: Rees, MI Fenton, I Williams, NM Holmans, P Norton, N Cardno, A Asherson, P Spurlock, G Roberts, E Parfitt, E Mant, P Vallada, H Dawson, E Li, MW Collier, DA Powell, JF Nanko, S Gill, M McGuffin, P Owen, MJ
Citation: Mi. Rees et al., Autosome search for schizophrenia susceptibility genes in multiply affected families, MOL PSYCHI, 4(4), 1999, pp. 353-359

Authors: Williams, NM Rees, MI Holmans, P Norton, N Cardno, AG Jones, LA Murphy, KC Sanders, RD McCarthy, G Gray, MY Fenton, I McGuffin, P Owen, MJ
Citation: Nm. Williams et al., A two-stage genome scan for schizophrenia susceptibility genes in 196 affected sibling pairs, HUM MOL GEN, 8(9), 1999, pp. 1729-1739

Authors: Kehoe, P Wavrant-De Vrieze, F Crook, R Wu, WS Holmans, P Fenton, I Spurlock, G Norton, N Williams, H Williams, N Lovestone, S Perez-Tur, J Hutton, M Chartier-Harlin, MC Shears, S Roehl, K Booth, J Van Voorst, W Ramic, D Williams, J Goate, A Hardy, J Owen, MJ
Citation: P. Kehoe et al., A full genome scan for late onset Alzheimer's disease, HUM MOL GEN, 8(2), 1999, pp. 237-245
Risultati: 1-6 |