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Results: 1-7 |
Results: 7

Authors: Visani, G Bernasconi, P Boni, M Castoldi, GL Ciolli, S Clavio, M Cox, MC Cuneo, A Del Poeta, G Dini, D Falzetti, D Fanin, R Gobbi, M Isidori, A Leoni, F Liso, V Malagola, M Martinelli, G Mecucci, C Piccaluga, PP Petti, MC Rondelli, R Russo, D Sessarego, M Specchia, G Testoni, N Torelli, G Mandelli, F Tura, S
Citation: G. Visani et al., The prognostic value of cytogenetics is reinforced by the kind of induction/consolidation therapy in influencing the outcome of acute myeloid leukemia - analysis of 848 patients, LEUKEMIA, 15(6), 2001, pp. 903-909

Authors: La Starza, R Aventin, A Falzetti, D Wlodarska, I Peralta, AMF Gonzalez-Aguilera, JJ Ciolli, S Martelli, MF Mecucci, C
Citation: R. La Starza et al., Regions of juxtaposition in unbalanced 1q rearrangements of malignant hemopathies, LEUKEMIA, 15(5), 2001, pp. 861-863

Authors: Ascoli, V Aalto, Y Carnovale-Scalzo, C Nardi, F Falzetti, D Mecucci, C Knuutila, S
Citation: V. Ascoli et al., DNA copy number changes in familial malignant mesothelioma, CANC GENET, 127(1), 2001, pp. 80-82

Authors: Falzetti, D Vermeesch, JR Matteucci, C Ciolli, S Martelli, MF Marynen, P Mecucci, C
Citation: D. Falzetti et al., Microdissection and FISH investigations in acute myeloid leukemia: A step forward to full identification of complex karyotypic changes, CANC GENET, 118(1), 2000, pp. 28-34

Authors: Falzetti, D Crescenzi, B Matteucci, C Falini, B Martelli, MF Van den Berghe, M Mecucci, C
Citation: D. Falzetti et al., Genomic instability and recurrent breakpoints are main cytogenetic findings in Hodgkin's disease, HAEMATOLOG, 84(4), 1999, pp. 298-305

Authors: Vermeesch, JR Duhamel, H Petit, P Falzetti, D Fryns, JP Marynen, P
Citation: Jr. Vermeesch et al., Multiple small accessory marker chromosomes from different centromeric origin in a moderately mentally retarded male, HUM GENET, 105(6), 1999, pp. 611-618

Authors: Falzetti, D Vermeesch, JR Hood, TL Nacheva, EP Matteucci, C Martelli, MF Van den Berghe, H Marynen, P Mecucci, C
Citation: D. Falzetti et al., Identification of multiple copies of a 20q-chromosome in a case of myelodysplastic syndrome: a FISH study, LEUK RES, 23(4), 1999, pp. 407-413
Risultati: 1-7 |