Authors:
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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:
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:
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
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
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