The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndrome von Minelli, A, Maserati, E, Nicolis, E, Zecca, M, Sainati, L, Longoni, D, Lo Curto, F, Menna, G, Poli, F, De Paoli, E, Cipolli, M, Locatelli, F, Pasquali, F, Danesino, C

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Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR von Porta, G, Maserati, E, Mattarucchi, E, Minelli, A, Pressato, B, Valli, R, Zecca, M, Bernardo, M E, Curto, F Lo, Locatelli, F, Danesino, C, Pasquali, F

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Erratum: OTX1 expression in breast cancer is regulated by p53 von Terrinoni, A, Pagani, I S, Zucchi, I, Chiaravalli, A M, Serra, V, Rovera, F, Sirchia, S, Dionigi, G, Miozzo, M, Frattini, A, Ferrari, A, Capella, C, Pasquali, F, Lo Curto, F, Albertini, A, Melino, G, Porta, G

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OTX1 expression in breast cancer is regulated by p53 von Terrinoni, A, Pagani, I S, Zucchi, I, Chiaravalli, A M, Serra, V, Rovera, F, Sirchia, S, Dionigi, G, Miozzo, M, Frattini, A, Ferrari, A, Capella, C, Pasquali, F, Lo Curto, F, Albertini, A, Melino, G, Porta, G

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Erratum: OTX1 expression in breast cancer is regulated by p53 von Terrinoni, A, Pagani, I S, Zucchi, I, Chiaravalli, A M, Serra, V, Rovera, F, Sirchia, S, Dionigi, G, Miozzo, M, Frattini, A, Ferrari, A, Capella, C, Pasquali, F, Lo Curto, F, Albertini, A, Melino, G, Porta, G

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OTX1 expression in breast cancer is regulated by p53 von Terrinoni, A, Pagani, I S, Zucchi, I, Chiaravalli, A M, Serra, V, Rovera, F, Sirchia, S, Dionigi, G, Miozzo, M, Frattini, A, Ferrari, A, Capella, C, Pasquali, F, Curto, F L, Albertini, A, Melino, G, Porta, G

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Indirect immunofluorescence of inactive centromeres as indicator of centromeric function von PERETTI, D, MARASCHIO, P, LAMBIASE, S, CURTO, F. L, ZUFFARDI, O

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Changes in glial fibrillary acidic protein and karyotype during culturing of two cell lines established from human glioblastoma multiforme von BOCCHINI, V, CASALONE, R, COLLINI, P, REBEL, G, LO CURTO, F

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Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498) von Maserati, Emanuela, Panarello, Claudio, Morerio, Cristina, Valli, Roberto, Pressato, Barbara, Patitucci, Francesco, Tassano, Elisa, Di Cesare-Merlone, Alessandra, Cugno, Chiara, Balduini, Carlo L, Lo Curto, Francesco, Dufour, Carlo, Locatelli, Franco, Pasquali, Francesco

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Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies von Maserati, Emanuela, Minelli, Antonella, Pressato, Barbara, Valli, Roberto, Crescenzi, Barbara, Stefanelli, Maurizio, Menna, Giuseppe, Sainati, Laura, Poli, Furio, Panarello, Claudio, Zecca, Marco, Curto, Francesco Lo, Mecucci, Cristina, Danesino, Cesare, Pasquali, Francesco

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OTX1 expression in breast cancer is regulated by p53 von Terrinoni, A, Pagani, I S, Zucchi, I, Chiaravalli, A M, Serra, V, Rovera, F, Sirchia, S, Dionigi, G, Miozzo, M, Frattini, A, Ferrari, A, Capella, C, Pasquali, F, Lo Curto, F, Albertini, A, Melino, G, Porta, G

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Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases von Maserati, Emanuela, Aprili, Fiorenza, Vinante, Fabrizio, Locatelli, Franco, Amendola, Giovanni, Zatterale, Adriana, Milone, Giuseppe, Minelli, Antonella, Bernardi, Franca, Lo Curto, Francesco, Pasquali, Francesco

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Cd bands and centromeric function in dicentric chromosomes von Maraschio, P, Zuffardi, O, Lo Curto, F

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Familial platelet disorder with propensity to acute myelogenous leukemia: Genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies von Minelli, Antonella, Maserati, Emanuela, Rossi, Gabriele, Bernardo, Maria Ester, De Stefano, Piero, Cecchini, Maria Paola, Valli, Roberto, Albano, Veronica, Pierani, Paolo, Leszl, Anna, Sainati, Laura, Lo Curto, Francesco, Danesino, Cesare, Locatelli, Franco, Pasquali, Francesco

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Insulin-like growth factors (IGF-I and IGF-II) and IGF-binding protein-3 production by fibroblasts of patients with Turner's syndrome in culture von BARRECA, A, LARIZZA, D, DAMONTE, G, ARVIGO, M, PONZANI, P, CESARONE, A, LO CURTO, F, SEVERI, F, GIORDANO, G, MINUTO, F

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The origin and phenotype of XO males von Fraccaro, M, Lindsten, J, Lo Curto, F

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Presumptive mosaic origin of an XX/XY female with ambiguous genitalia von Zuffardi, O, Gargantini, L, Lambiase, S, Lo Curto, F, Maraschio, P, Ford, C E

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Letter: Nuclear projections in tumour cells von Lo Curto, F, Fraccaro, M

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Correlation between the number of sex chromosomes and the H-Y antigen titer von Fraccaro, M, Mayerová, A, Wolf, U, Bühler, E, Gebauer, J, Gilgenkrantz, S, Lindsten, J, Lo Curto, F, Ritzén, E M

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A woman carrier of two apparently unrelated reciprocal translocations: prenatal diagnosis of normal karyotype in the foetus von Simoni, G, Montali, E, Rossella, F, Dalprà, L, Lo Curto, F

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