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Titolo Data di pubblicazione Autore(i) File
Orign and clinical significance of inv dup(15) 1-gen-1988 Maraschio, Paola; Cuoco, C; Gimelli, G; Zuffardi, Orsetta; Tiepolo, Luciano
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome. 1-gen-1989 Ballabio, A; Andria, G; Carrozzo, R; Persico, G; Bick, D; Campbell, L; Ropers, Hh; FERGUSON SMITH, Ma; Gimelli, G; Fraccaro, M; Maraschio, Paola; Zuffardi, Orsetta; Bardoni, B; Guioli, S; Camerino, Giovanna
Alternate centromere inactivation in a pseudodicentric (15;20) associated with a progressive neurological disorder 1-gen-1989 Rivera, H; Zuffardi, Orsetta; Maraschio, Paola; Caiulo, A; Anichini, C; Scarinci, R; Vivarelli, R.
Evidence for human mitotic mutant with pleiotropic effect 1-gen-1989 Papi, L; Montali, E; Marconi, G; Bigozzi, U; Maraschio, Paola; Zuffardi, Orsetta
Regional assignment of the loci for adenylate kinase to 9q32 and for alfa1 acid glycoprotein to 9q31-q32 1-gen-1989 Zuffardi, Orsetta; Caiulo, A; Maraschio, Paola; Tupler, R; Bianchi, E; Amisano, P; Beluffi, G; Moratti, R; Liguri, G.
Deletion of specific sequence or modification of centromeric chromatin are responsible for Y chromosome centromere inactivation 1-gen-1990 Maraschio, Paola; Zuffardi, Orsetta; Caiulo, A; Dainotti, E; Piantanida, M; Rivera, H; Tupler, R.
Chromosome abnormalities in lymphocytes and fibroblasts of subjects with multiple endocrine neoplasia type 1. 1-gen-1991 Scappaticci, MARIA ASSUNTA; Maraschio, Paola; del Ciotto, N; Fossati, Gs; Zonta, Aris; Fraccaro, Marco
The modes of Y chromosome centromere inactivation in pseudodicentric chromosomes 1-gen-1991 Maraschio, Paola; Zuffardi, Orsetta; Caiulo, A; Dainotti, E; Tupler, R; Piantanida, M.
Mapping the gene encoding the human erythroid transcriptonal factor NFE1-GF1 to Xp11-23 1-gen-1991 Caiulo, A; Nicolis, S; Bianchi, P; Zuffardi, Orsetta; Bardoni, B; Maraschio, Paola; Ottolenghi, S; Camerino, G; Giglioni, G.
Cytogenetics of multiple endocrine neoplasia syndrome. II. Chromosome abnormalities in an insulinoma and a Glaucoma from two subjects with MEN1. 1-gen-1992 Scappaticci, MARIA ASSUNTA; Brandi, Ml; Capra, E; Cortinovis, M; Maraschio, Paola; Fraccaro, Marco
Cytogenetic of multiple endocrine neoplasia syndromes. I. Two different, unique clonal chromosome changes in a medullary thyroid carcinoma and in a C-cell thyroid hyperplasia. 1-gen-1992 Scappaticci, MARIA ASSUNTA; Arrigoni, G; Capra, E; Maraschio, Paola; Fraccaro, Marco
Anticentroameric antibodies and inactive centromeres 1-gen-1996 Zuffardi, Orsetta; Maraschio, Paola; Peretti, Diletta; Lambiase, Simonetta; LO CURTO, Francesco
A novel mechnaism for the origin of supernumerary marker chromosomes 1-gen-1996 Maraschio, Paola; Tupler, R; Rossi, Elena; Barbierato, L; Uccellatore, F; Rocchi, M; Zuffardi, Orsetta; Fraccaro, Marco
A variant of the Nijmegen breakage syndrome with unusual cytogenetic features and intermediate cellular radiosensitivity 1-gen-1997 Tupler, R.; Marseglia, GIAN LUIGI; Stefanini, M.; Prosperi, E.; Chessa, L.; Nardo, T.; Marchi, Antonietta; Maraschio, Paola
Ring chromosome 9 with a 9p22.3-p24.3 duplication 1-gen-1999 Seghezzi, L; Maraschio, Paola; Bozzola, Mauro; Maserati, E; Tupler, R; Marchi, Antonietta; Tiepolo, R.
A novel mutation and novel features in Nijmegen breakage syndrome. 1-gen-2001 Maraschio, Paola; Danesino, Cesare; Antoccia, A; Ricordy, R; Tanzarella, C; Varon, R; Reis, A; Besana, D; Guala, A; Tiepolo, Luciano
Comment on: Corpus callosum hypoplasia and associated brain anomalies in Nijmegen breakage syndrome. 1-gen-2002 Maraschio, Paola; Danesino, Cesare; Varon, R; Tiepolo, Luciano
Genetic heterogeneity for a Nijmegen Breakage-like Syndrome 1-gen-2003 Maraschio, Paola; Spadoni, Emanuela; Tanzarella, C.; Antoccia, A.; DI MASI, A.; Maghnie, M.; Varon, R.; Demuth, I.; Tiepolo, Luciano; Danesino, Cesare
Interstitial deletion of chromsome 9, int del(9)(9q22.31-q31.2), including the genes causing multiple basal cell nevus syndrome and Robinow/brachydactyly 1 syndrome. 1-gen-2003 Olivieri, Carla; Maraschio, Paola; D., Caselli; C., Martini; G., Beluffi; E., Maserati; Danesino, Cesare
Chromosome instability and nibrin protein variants in NBS heterozygotes. 1-gen-2003 Tanzarella, C; Antoccia, A; Spadoni, E; di Masi, A; Pecile, V; Demori, E; Varon, R; Marseglia, GIAN LUIGI; Tiepolo, Luciano; Maraschio, Paola
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