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Results: 1-6 |
Results: 6

Authors: Kovacs, GG Ertsey, C Majtenyi, C Jelencsik, I Laszlo, L Flicker, H Strain, L Szirmai, I Budka, H
Citation: Gg. Kovacs et al., Inherited prion disease with A117V mutation of the prion protein gene: a novel Hungarian family, J NE NE PSY, 70(6), 2001, pp. 802-805

Authors: Bonthron, DT Hayward, BE Moran, V Strain, L
Citation: Dt. Bonthron et al., Characterization of TH1 and CTSZ, two non-imprinted genes downstream of GNAS1 in chromosome 20q13, HUM GENET, 107(2), 2000, pp. 165-175

Authors: Judson, H van Roy, N Strain, L Vandesompele, J Van Gele, M Speleman, F Bonthron, DT
Citation: H. Judson et al., Structure and mutation analysis of the gene encoding DNA fragmentation factor 40 (caspase-activated nuclease), a candidate neuroblastoma tumour suppressor gene, HUM GENET, 106(4), 2000, pp. 406-413

Authors: McDowell, I Hill, G Lindsay, J Helliwell, B Chappell, N Tuokko, H Beattie, BL Feldman, H Sadovnick, D Gutman, G Hogan, DB Bland, R McCracken, P Newman, S D'Arcy, C Manfreda, J Montgomery, P Strain, L Ostbye, T Steenhuis, R Hachinski, V Chambers, L Raina, P Braun, A Patterson, C Cohen, C Colantonio, A Snow, G Kozak, J Wolfson, C Gauthier, S Bergman, H Panisset, M Ska, B Kergoat, MJ Joanette, Y Hebert, R Verreault, R Durand, P Morin, J Morin, M Bouchard, R Gauvreau, D Fortier, I Balram, C Rockwood, K Graham, J Fisk, J MacKnight, C Nilsson, T Pedlar, D Buehler, S Kozma, A
Citation: I. Mcdowell et al., The incidence of dementia in Canada, NEUROLOGY, 55(1), 2000, pp. 66-73

Authors: Moore, SJ Strain, L Cole, GF Miedzybrodzka, Z Kelly, KF Dean, JCS
Citation: Sj. Moore et al., Fragile X syndrome with FMR1 and FMR2 deletion, J MED GENET, 36(7), 1999, pp. 565-566

Authors: Hayward, BE Moran, V Strain, L Bonthron, DT
Citation: Be. Hayward et al., Bidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally, and biallelically derived proteins, P NAS US, 95(26), 1998, pp. 15475-15480
Risultati: 1-6 |