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Results: 1-17 |
Results: 17

Authors: Lopez-Urrutia, JRC Bapat, B Draganic, I Werdich, A Ullrich, J
Citation: Jrc. Lopez-urrutia et al., First results from the freiburg electron beam ion trap FreEBIT, PHYS SCR, T92, 2001, pp. 110-112

Authors: Esplen, MJ Madlensky, L Butler, K McKinnon, W Bapat, B Wong, JH Aronson, M Gallinger, S
Citation: Mj. Esplen et al., Motivations and psychosocial impact of genetic testing for HNPCC, AM J MED G, 103(1), 2001, pp. 9-15

Authors: Percin, EF Ploder, LA Yu, JJ Arici, K Horsford, DJ Rutherford, A Bapat, B Cox, DW Duncan, AMV Kalnins, VI Kocak-Altintas, A Sowden, JC Traboulsi, E Sarfarazi, M McInnes, RR
Citation: Ef. Percin et al., Human microphthalmia associated with mutations in the retinal homeobox gene CHX10, NAT GENET, 25(4), 2000, pp. 397-401

Authors: Bapat, B Keller, S Moshammer, R Mann, R Ullrich, J
Citation: B. Bapat et al., Double ionization of helium in fast ion collisions: the role of the correlated initial state, J PHYS B, 33(7), 2000, pp. 1437-1446

Authors: Keller, S Bapat, B Moshammer, R Ullrich, J Dreizler, RM
Citation: S. Keller et al., Double ionization of helium in fast ion collisions: comparative study of model wavefunctions, J PHYS B, 33(7), 2000, pp. 1447-1461

Authors: Charames, GS Millar, AL Pal, T Narod, S Bapat, B
Citation: Gs. Charames et al., Do MSH6 mutations contribute to double primary cancers of the colorectum and endometrium?, HUM GENET, 107(6), 2000, pp. 623-629

Authors: Lopez-Urrutia, JRC Bapat, B Feuerstein, B Werdich, A Ullrich, J
Citation: Jrc. Lopez-urrutia et al., First results from the Freiburg electron beam ion trap FreEBIT, HYPER INTER, 127(1-4), 2000, pp. 497-501

Authors: Moshammer, R Schulz, M Schmitt, W Kollmus, H Mann, R Bapat, B Hagmann, S Fainstein, PD Olson, RE Ullrich, J
Citation: R. Moshammer et al., Kinematically complete ion-atom collision experiments: Ionization of atomsin strong fields, AIP CONF PR, 500, 2000, pp. 571-580

Authors: Couture, J Mitri, A Lagace, R Smits, R Berk, T Bouchard, HL Fodde, R Alman, B Bapat, B
Citation: J. Couture et al., A germline mutation at the extreme 3 ' end of the APC gene results in a severe desmoid phenotype and is associated with overexpression of beta-catenin in the desmoid tumor, CLIN GENET, 57(3), 2000, pp. 205-212

Authors: Millar, AL Pal, T Madlensky, L Sherman, C Temple, L Mitri, A Cheng, H Marcus, V Gallinger, S Redston, M Bapat, B Narod, S
Citation: Al. Millar et al., Mismatch repair gene defects contribute to the genetic basis of double primary cancers of the colorectum and endometrium, HUM MOL GEN, 8(5), 1999, pp. 823-829

Authors: Bapat, B Moshammer, R Keller, S Schmitt, W Cassimi, A Adoui, L Kollmus, H Dorner, R Weber, T Khayyat, K Mann, R Grandin, JP Ullrich, J
Citation: B. Bapat et al., Double ionization of helium in fast ion collisions: the role of momentum transfer, J PHYS B, 32(8), 1999, pp. 1859-1872

Authors: Tejpar, S Nollet, F Li, C Wunder, JS Michils, G dal Cin, P Van Cutsem, E Bapat, B van Roy, F Cassiman, JJ Alman, BA
Citation: S. Tejpar et al., Predominance of beta-catenin mutations and beta-catenin dysregulation in sporadic aggressive fibromatosis (desmoid tumor), ONCOGENE, 18(47), 1999, pp. 6615-6620

Authors: Bapat, B Moshammer, R Schmitt, W Kollmus, H Mann, R Dorner, R Weber, T Khayyat, K Cassimi, A Adoui, L Grandin, JP Ullrich, J
Citation: B. Bapat et al., Double ionization of helium by fast fully stripped ions, PHYS SCR, T80B, 1999, pp. 351-353

Authors: Bapat, B Noorani, H Cohen, Z Berk, T Mitri, A Gallie, B Pritzker, K Gallinger, S Detsky, AS
Citation: B. Bapat et al., Cost comparison of predictive genetic testing versus conventional clinicalscreening for familial adenomatous polyposis, GUT, 44(5), 1999, pp. 698-703

Authors: Berk, T Cohen, Z Bapat, B Gallinger, S
Citation: T. Berk et al., Negative genetic test result in familial adenomatous polyposis - Clinical screening implications, DIS COL REC, 42(3), 1999, pp. 307-310

Authors: Jiang, CY Esufali, S Berk, T Gallinger, S Cohen, Z Tobi, M Redston, M Bapat, B
Citation: Cy. Jiang et al., STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients, CLIN GENET, 56(2), 1999, pp. 136-141

Authors: Mirabelli-Primdahl, L Gryfe, R Kim, H Millar, A Luceri, C Dale, D Holowaty, E Bapat, B Gallinger, S Redston, M
Citation: L. Mirabelli-primdahl et al., beta-catenin mutations are specific for colorectal carcinomas with microsatellite instability but occur in endometrial carcinomas irrespective of mutator pathway, CANCER RES, 59(14), 1999, pp. 3346-3351
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