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Results: 1-6 |
Results: 6

Authors: Rajcan-Separovic, E Robinson, WP Stephenson, M Pantzar, T Arbour, L McFadden, D Guscott, J
Citation: E. Rajcan-separovic et al., Recurrent trisomy 15 in a female carrier of der(15)t(Y;15)(q12;p13), AM J MED G, 99(4), 2001, pp. 320-324

Authors: Rahman, N Arbour, L Houlston, R Bonaiti-Pellie, C Abidi, F Tranchemontagne, J Ford, D Narod, S Pritchard-Jones, K Foulkes, WD Schwartz, C Stratton, MR
Citation: N. Rahman et al., Penetrance of mutations in the familial Wilms tumor gene FWT1, J NAT CANC, 92(8), 2000, pp. 650-652

Authors: Christensen, B Arbour, L Tran, P Leclerc, D Sabbaghian, N Platt, R Gilfix, BM Rosenblatt, DS Gravel, RA Forbes, P Rozen, R
Citation: B. Christensen et al., Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects, AM J MED G, 84(2), 1999, pp. 151-157

Authors: Bishai, R Arbour, L Lyones, C Koren, G
Citation: R. Bishai et al., Intrauterine exposure to clomiphene and neonatal persistent hyperplastic primary vitreous, TERATOLOGY, 60(3), 1999, pp. 143-145

Authors: Shkolny, DL Beitel, LK Ginsberg, J Pekeles, G Arbour, L Pinsky, L Trifiro, MA
Citation: Dl. Shkolny et al., Discordant measures of androgen-binding kinetics in two mutant androgen receptors causing mild or partial androgen insensitivity, respectively, J CLIN END, 84(2), 1999, pp. 805-810

Authors: Rahman, N Abidi, F Ford, D Arbour, L Rapley, E Tonin, P Barton, D Batcup, G Berry, J Cotter, F Davison, V Gerrard, M Gray, E Grundy, R Hanafy, M King, D Lewis, I Luethy, AR Madlensky, L Mann, J O'Meara, A Oakhill, T Skolnick, M Strong, L Variend, D Narod, S Schwartz, C Pritchard-Jones, K Stratton, MR
Citation: N. Rahman et al., Confirmation of FWT1 as a Wilms' tumour susceptibility gene and phenotypiccharacteristics of Wilms' tumour attributable to FWT1, HUM GENET, 103(5), 1998, pp. 547-556
Risultati: 1-6 |