ORZAN, FRANCESCA
ORZAN, FRANCESCA
Universita' degli Studi di MILANO
Evaluation of 1p36 markers and clinical outcome in a skull base chordoma study
2008 M. Longoni, F. Orzan, M. Stroppi, N. Boari, P. Mortini, P. Riva
Breakpoint characterization of a novel NF1 multiexonic deletion : a case showing expression of the mutated allele
2008 F. Orzan, M. Stroppi, M. Venturin, M.C. Valero, C. Hernández, P. Riva
Uncommon Alu-mediated NF1 microdeletion with a breakpoint inside the NF1 gene
2005 C. Gervasini, M. Venturin, F. Orzan, A. Friso, M. Clementi, R. Tenconi, L. Larizza, P. Riva
Evidence for nonhomologous end joining and non allelic homologous recombination in atypical NF1 microdeletions
2004 M. Venturin , C. Gervasini, F. Orzan, A. Bentivegna, L. Corrado, P. Colapietro , A. Friso, R. Tenconi, M. Upadhyaya, L. Larizza, P. Riva
Mapping of candidate region for chordoma development to 1p36.13 by LOH analysis
2003 P. Riva, F. Crosti, F. Orzan, L. Dalprà, P. Mortini, A. Parafioriti, B. Pollo, A.M. Fuhrman Conti, M. Miozzo, L. Larizza
Genotype-phenotype correlation in patients with NF1 microdeletion syndrome : identification of candidate genes for mental retardation
2002 P. Riva, M. Venturin, P. Guarnieri, F. Orzan, F. Natacci, C. Gervasini, P. Colapietro, A. Bentivegna, R. Stabile, R. Tenconi, M. Upadhyaya, C. Hernandez, L. Larizza