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Results: 1-6 |
Results: 6

Authors: Fromont-Racine, M Mayes, AE Brunet-Simon, A Rain, JC Colley, A Dix, I Decourty, L Joly, N Ricard, F Beggs, JD Legrain, P
Citation: M. Fromont-racine et al., Genome-wide protein interaction screens reveal functional networks involving Sm-like proteins, YEAST, 17(2), 2000, pp. 95-110

Authors: Colley, A Beggs, JD Tollervey, D Lafontaine, DLJ
Citation: A. Colley et al., Dhr1p, a putative DEAH-Box RNA helicase, is associated with the box C+D snoRNP U3, MOL CELL B, 20(19), 2000, pp. 7238-7246

Authors: Meiser, B Butow, P Barratt, A Suthers, G Smith, M Colley, A Thompson, E Tucker, K
Citation: B. Meiser et al., Attitudes to genetic testing for breast cancer susceptibility in women at increased risk of developing hereditary breast cancer, J MED GENET, 37(6), 2000, pp. 472-476

Authors: Gedeon, AK Colley, A Jamieson, R Thompson, EM Rogers, J Sillence, D Tiller, GE Mulley, JC Gecz, J
Citation: Ak. Gedeon et al., Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda, NAT GENET, 22(4), 1999, pp. 400-404

Authors: Friend, KL Crimmins, D Phan, TG Sue, CM Colley, A Fung, VSC Morris, JGL Sutherland, GR Richards, RI
Citation: Kl. Friend et al., Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM, HUM GENET, 105(3), 1999, pp. 261-265

Authors: McQuade, L Christodoulou, J Budarf, M Sachdev, R Wilson, M Emanuel, B Colley, A
Citation: L. Mcquade et al., Patient with a 22q11.2 deletion with no overlap of the minimal DiGeorge syndrome critical region (MDGCR), AM J MED G, 86(1), 1999, pp. 27-33
Risultati: 1-6 |