A novel spinocerebellar ataxia type 15 family with involuntary movements and cognitive decline von Castrioto, A., Prontera, P., Di Gregorio, E., Rossi, V., Parnetti, L., Rossi, A., Donti, E., Brusco, A., Calabresi, P., Tambasco, N.

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Aicardi Syndrome Associated with Autosomal Genomic Imbalance: Coincidence or Evidence for Autosomal Inheritance with Sex-Limited Expression? von Prontera, P., Bartocci, A., Ottaviani, V., Isidori, I., Rogaia, D., Ardisia, C., Guercini, G., Mencarelli, A., Donti, E.

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Translocation Breakpoint of Acute Promyelocytic Leukemia Lies Within the Retinoic Acid Receptor α Locus von Alcalay, Myriam, Zangrilli, Daniela, Pandolfi, Pier Paolo, Longo, Letizia, Mencarelli, Amedea, Giacomucci, angelo, Rocchi, Mariano, Biondi, Andrea, Rambaldi, Alessandro, Lo Coco, Francesco, Diverio, Daniela, Donti, Emilio, Grignani, Fausto, Pelicci, Pier Giuseppe

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Blood cell mitochondrial DNA content and premature ovarian aging von Bonomi, Marco, Somigliana, Edgardo, Cacciatore, Chiara, Busnelli, Marta, Rossetti, Raffaella, Bonetti, Silvia, Paffoni, Alessio, Mari, Daniela, Ragni, Guido, Persani, Luca

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The Italian External Quality Assessment Scheme in Classical Cytogenetics: Four Years of Activity von Floridia, G., Falbo, V., Censi, F., Tosto, F., Salvatore, M., Baroncini, A., Battaglia, P., Conti, A., Donti, E., La Starza, R., Nitsch, L., Pierluigi, M., Piombo, G., Susca, F., Mancini, M., Mecucci, C., Calzolari, E., Bricarelli, F. Dagna, Guanti, G., Taruscio, D.

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MASA syndrome: ultrasonographic evidence in a male fetus von Pomili, G., Venti Donti, G., Alunni Carrozza, L., Ardisia, C., Servidio, F., Hofstra, R. M. W., Gilardi, G., Donti, E.

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Persistence of chromosomal abnormalities additional to the Philadelphia chromosome after Philadelphia chromosome disappearance during imatinib therapy for chronic myeloid leukemia von Zaccaria, Alfonso, Valenti, Anna Maria, Donti, Emilio, Gozzetti, Alessandro, Ronconi, Sonia, Spedicato, Francesco

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Interferon Alpha-2b as Therapy for Ph'-Positive Chronic Myelogenous Leukemia: A Study of 82 Patients Treated With Intermittent or Daily Administration von Alimena, Giuliana, Morra, Enrica, Lazzarino, Mario, Liberati, Anna M., Montefusco, Enrico, Inverardi, Daniela, Bernasconi, Paolo, Mancini, Marco, Donti, Emilio, Grignani, Fausto, Bernasconi, Carlo, Dianzani, Ferdinando, Mandelli, Franco

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A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure von Corre, Tanguy, Schuettler, Julia, Bione, Silvia, Marozzi, Anna, Persani, Luca, Rossetti, Raffaella, Torricelli, Francesca, Giotti, Irene, Vogt, Peter, Toniolo, Daniela

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Acute promyelocytic leukemia: from genetics to treatment von Grignani, F, Fagioli, M, Alcalay, M, Longo, L, Pandolfi, PP, Donti, E, Biondi, A, Lo Coco, F, Pelicci, PG

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Acute Promyelocytic Leukemia: From Genetics to Treatment von Grignani, Francesco, Fagioli, Marta, Alcalay, Myriam, Longo, Letizia, Pandolfi, Pier Paolo, Donti, Emilio, Biondi, Andrea, Coco, Francesco Lo, Grignani, Fausto, Pelicci, Pier Giuseppe

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Prenatal Diagnosis in Italy von Clerici, G., Donti, E., Zacutti, A., Di Renzo, G.C.

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Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: Cooperative study of 19 Italian laboratories von Dalprà, Leda, Giardino, Daniela, Finelli, Palma, Corti, Cecilia, Valtorta, Chiara, Guerneri, Silvana, Ilardi, Patrizia, Fortuna, Renato, Coviello, Domenico, Nocera, Gianfranco, Amico, Francesco Paolo, Martinoli, Emanuela, Sala, Elena, Villa, Nicoletta, Crosti, Francesca, Chiodo, Francamaria, di Cantogno, Ludovica Verdun, Savin, Elisa, Croci, Gianfranco, Franchi, Fabrizia, Venti, Giovanna, Donti, Emilio, Migliori, Valeria, Pettinari, Antonella, Bonifacio, Stefania, Centrone, Claudia, Torricelli, Francesca, Rossi, Simona, Simi, Paolo, Granata, Paola, Casalone, Rosario, Lenzini, Elisabetta, Artifoni, Lina, Pecile, Vanna, Barlati, Sergio, Bellotti, Daniela, Caufin, Daniele, Police, Adalgisa, Cavani, Simona, Piombo, Giuseppe, Pierluigi, Mauro, Larizza, Lidia

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PTH induces modification of transductive events in otosclerotic bone cell cultures von Fanó, G., Venti-Donti, G., Belia, S., Paludetti, G., Antonica, A., Donti, E., Maurizi, M.

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Glycosaminoglycan metabolism in otosclerotic bone cells von Locci, P, Becchetti, E, Venti, G, Lilli, C, Marinucci, L, Donti, E, Paludetti, G, Maurizi, M

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Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders von Sabatino, G., Calabrese, G., Franchi, P.Guanciali, Stuppia, L., Jadayel, D., Donti, E., Palka, G.

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Glycosaminoglycan metabolism in otosclerotic bone cells von Locci, P., Becchetti, E., Venti, G., Lilli, C., Marinucci, L., Donti, E., Paludetti, G., Maurizi, M.

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Altered adenylate cyclase activity in human otosclerotic bone cell cultures von Torre, G.Delia, Fulle, S., Donti, G.Venti, Paludetti, G., Maurizi, M., Donti, E., Fanò, G.

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Morphological and functional characteristics of human temporal-bone cell cultures von Maurizi, M, Binaglia, L, Donti, E, Ottaviani, F, Paludetti, G, Venti Donti, G

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A new human highly tumorigenic neuroblastoma cell line with undetectable expression of N-myc von CORNAGLIA-FERRARIS, P, PONZONI, M, MONTALDO, P, MARIOTTINI, G. L, DONTI, E, DI MARTINO, D, TONINI, G. P

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