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Results: 1-13 |
Results: 13
Refinement within single yeast artificial chromosome clones of a minimal region commonly deleted on the short arm of chromosome 7 in Wilms tumours
Authors: Perotti, D Testi, MA Mondini, P Pilotti, S Green, ED Pession, A Sozzi, G Pierotti, MA Fossati-Bellani, F Radice, P
Citation: D. Perotti et al., Refinement within single yeast artificial chromosome clones of a minimal region commonly deleted on the short arm of chromosome 7 in Wilms tumours, GENE CHROM, 31(1), 2001, pp. 42-47
Genotype and phenotype factors as determinants of desmoid tumors in patients with familial adenomatous polyposis
Authors: Bertario, L Russo, A Sala, P Eboli, M Giarola, M D'Amico, F Gismondi, V Varesco, L Pierotti, MA Radice, P
Citation: L. Bertario et al., Genotype and phenotype factors as determinants of desmoid tumors in patients with familial adenomatous polyposis, INT J CANC, 95(2), 2001, pp. 102-107
Ileorectal anastomosis in patients with familial adenomatous polyposis
Authors: Bertario, L Sala, P Radice, P Russo, A
Citation: L. Bertario et al., Ileorectal anastomosis in patients with familial adenomatous polyposis, GASTROENTY, 121(2), 2001, pp. 502-502
Detection of germline BRCA1 mutations by multiple-dye cleavase fragment length polymorphism (MD-CFLP) method
Authors: Casadei, S Cortesi, L Pensotti, V Radice, P Pierotti, M Amadori, D Calistri, D
Citation: S. Casadei et al., Detection of germline BRCA1 mutations by multiple-dye cleavase fragment length polymorphism (MD-CFLP) method, BR J CANC, 85(6), 2001, pp. 845-849
A novel zinc finger gene is fused to EWS in small round cell tumor
Authors: Mastrangelo, T Modena, P Tornielli, S Bullrich, F Testi, MA Mezzelani, A Radice, P Azzarelli, A Pilotti, S Croce, CM Pierotti, MA Sozzi, G
Citation: T. Mastrangelo et al., A novel zinc finger gene is fused to EWS in small round cell tumor, ONCOGENE, 19(33), 2000, pp. 3799-3804
Recurrent germline mutation in MSH2 arises frequently de novo
Authors: Desai, DC Lockman, JC Chadwick, RB Gao, X Percesepe, A Evans, DGR Miyaki, M Yuen, ST Radice, P Maher, ER Wright, FA de la Chapelle, A
Citation: Dc. Desai et al., Recurrent germline mutation in MSH2 arises frequently de novo, J MED GENET, 37(9), 2000, pp. 646-652
Microsatellite instability in colorectal-cancer patients with suspected genetic predisposition
Authors: Calistri, D Presciuttini, S Buonsanti, G Radice, P Gazzoli, I Pensotti, V Sala, P Eboli, M Andreola, S Russo, A Pierotti, M Bertario, L Ranzani, GN
Citation: D. Calistri et al., Microsatellite instability in colorectal-cancer patients with suspected genetic predisposition, INT J CANC, 89(1), 2000, pp. 87-91
Genotype and phenotype factors as determinants for rectal stump cancer in patients with familial adenomatous polyposis
Authors: Bertario, L Russo, A Radice, P Varesco, L Eboli, M Spinelli, P Reyna, A Sala, P
Citation: L. Bertario et al., Genotype and phenotype factors as determinants for rectal stump cancer in patients with familial adenomatous polyposis, ANN SURG, 231(4), 2000, pp. 538-543
The exon 13 duplication in the BRCA1 gene is a founder mutation present ingeographically diverse populations
Authors: Mazoyer, S Leary, J Kirk, J Fleischmann, E Wagner, T Claes, K Messiaen, L Foulkes, W Desrochers, M Simard, J Phelan, CM Kwan, E Narod, SA Vahteristo, P Nevanlinna, H Durando, X Bignon, YJ Peyrat, JP Bonnardel, C Sinilnikova, OM Puget, N Lenoir, GM Mazoyer, S Audoynaud, C Goldgar, D Maugard, C Caux, V Gad, S Stoppa-Lyonnet, D Nogues, C Lidereau, R Machavoine, C Bressac-de Paillerets, B Kuschel, B Betz, B Niederacher, D Beckmann, MW Hamann, U Gayther, SA Ponder, BAP Robinson, M Taylor, GR Bishop, T Catteau, A Solomon, E Cohen, B Steel, M Collins, N Stratton, M van der Looij, M Olah, E Miller, NJ Barton, DE Sverdlov, RS Friedman, E Radice, P Montagna, M Sensi, E Caligo, M van Eijk, R Devilee, P van der Luijt, R Heimdal, K Moller, P Borg, A Diez, O Cortes, J Domenech, M Baiget, M Osorio, A Benitez, J Borg, A Maillet, P Sappino, AP Ozdag, H Ozcelik, T Ozturk, M Rohlfs, EM Boyd, J McDermott, D Offit, K Unger, M Nathanson, K Weber, BL Sellers, TA Hampton, E Couch, FJ Neuhausen, S
Citation: S. Mazoyer et al., The exon 13 duplication in the BRCA1 gene is a founder mutation present ingeographically diverse populations, AM J HU GEN, 67(1), 2000, pp. 207-212
Algorithm to correct hyperopic astigmatism with the Nidek EC-5000 excimer laser
Authors: Vinciguerra, P Epstein, D Azzolini, M Radice, P Sborgia, M
Citation: P. Vinciguerra et al., Algorithm to correct hyperopic astigmatism with the Nidek EC-5000 excimer laser, J REFRACT S, 15(2), 1999, pp. S186-S187
Screening for mutations of the APC gene in 66 Italian familial adenomatouspolyposis patients: Evidence for phenotypic differences in cases with and without identified mutation
Authors: Giarola, M Stagi, L Presciuttini, S Mondini, P Radice, MT Sala, P Pierotti, MA Bertario, L Radice, P
Citation: M. Giarola et al., Screening for mutations of the APC gene in 66 Italian familial adenomatouspolyposis patients: Evidence for phenotypic differences in cases with and without identified mutation, HUM MUTAT, 13(2), 1999, pp. 116-123
Survival of patients with hereditary colorectal cancer: Comparison of HNPCC and colorectal cancer in FAP patients with sporadic colorectal cancer
Authors: Bertario, L Russo, A Sala, P Eboli, M Radice, P Presciuttini, S Andreola, S Rodriguez-Bigas, MA Pizzetti, P Spinelli, P
Citation: L. Bertario et al., Survival of patients with hereditary colorectal cancer: Comparison of HNPCC and colorectal cancer in FAP patients with sporadic colorectal cancer, INT J CANC, 80(2), 1999, pp. 183-187
A novel EWS-ERG rearrangement generating two hybrid mRNAs in a peripheral primitive neuroectodermal tumour (PPNET) with a t(15;22) translocation
Authors: Minoletti, F Sozzi, G Tornielli, S Pilotti, S Azzarelli, A Pierotti, MA Radice, P
Citation: F. Minoletti et al., A novel EWS-ERG rearrangement generating two hybrid mRNAs in a peripheral primitive neuroectodermal tumour (PPNET) with a t(15;22) translocation, J PATHOLOGY, 186(4), 1998, pp. 434-437
Risultati: 1-13 |