Scoliosis with cognitive impairment in a girl with 8q11.21q11.23 microdeletion and SNTG1 disruption von Tassano, E., Ronchetto, P., Severino, M., Divizia, M.T., Lerone, M., Uccella, S., Nobili, L., Tavella, E., Morerio, C., Coviello, D., Malacarne, M.

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17q23.3 de novo microdeletion involving only TANC2 gene: A new case von Tassano, E., Accogli, A., Ronchetto, P., Tortora, D., Tavella, E., Gimelli, G., Mancardi, M., Malacarne, M., Coviello, D.A.

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De novo 13q31.1-q32.1 interstitial deletion encompassing the miR-17-92 cluster in a patient with Feingold syndrome-2 von Tassano, E., Di Rocco, M., Signa, S., Gimelli, G.

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Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations von Villa, R., Fergnani, V.G.C., Silipigni, R., Guerneri, S., Cinnante, C., Guala, A., Danesino, C., Scola, E., Conte, G., Fumagalli, M., Gangi, S., Colombo, L., Picciolini, O., Ajmone, P.F., Accogli, A., Madia, F., Tassano, E., Scala, M., Capra, V., Srour, M., Spaccini, L., Righini, A., Greco, D., Castiglia, L., Romano, C., Bedeschi, M.F.

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Pituitary deficiency and congenital infiltrating lipomatosis of the face in a girl with deletion of chromosome 1q24.3q31.1 von Capra, V., Severino, M., Rossi, A., Nozza, P., Doneda, C., Perri, K., Pavanello, M., Fiorio, P., Gimelli, G., Tassano, E., Di Battista, E.

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Interstitial deletion 14q31.1q31.3 transmitted from a mother to her daughter, both with features of hemifacial microsomia von Gimelli, S., Cuoco, C., Ronchetto, P., Gimelli, G., Tassano, E.

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Molecular cytogenetic characterization of the first reported case of an inv dup (4p)(p15.1-pter) with a concomitant 4q35.1-qter deletion and normal parents von Tassano, E., Alpigiani, M.G., Salvati, P., Gimelli, S., Lorini, R., Gimelli, G.

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Clinical and molecular delineation of a 16p13.2p13.13 microduplication von Tassano, E, Alpigiani, M.G, Calcagno, A, Salvati, P, De Miglio, L, Fiorio, P, Cuoco, C, Gimelli, G

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PD-0499 Optimising cervix brachytherapy planning using OAR dose estimates from external beam RT daily CBCTs von Tassano-Smith, E., Palmer, A.L., Polak, W.

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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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Reduced systolic performance by tissue Doppler in patients with preserved and abnormal ejection fraction: New insights in chronic heart failure von García, Edgar H., Perna, Eduardo R., Farías, Eduardo F., Obregón, Ricardo O., Macin, Stella M., Parras, Jorge I., Agüero, Marcelo A., Moratorio, Diego A., Pitzus, Ariel E., Tassano, Eduardo A., Rodriguez, Leonardo

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t(9;11)(p22;p15) with NUP98-LEDGF fusion gene in pediatric acute myeloid leukemia von Morerio, Cristina, Acquila, Maura, Rosanda, Cristina, Rapella, Annamaria, Tassano, Elisa, Micalizzi, Concetta, Panarello, Claudio

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MLL– MLLT10 fusion gene in pediatric acute megakaryoblastic leukemia von Morerio, Cristina, Rapella, Annamaria, Tassano, Elisa, Rosanda, Cristina, Panarello, Claudio

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LONGITUDINAL CONTRACTION OF LEFT VENTRICLE WITH INOTROPIC STIMULATION WITH DOBUTAMINE BY TISSUE DOPPLER. CORRELATION WITH EJECTION FRACTION IN NORMAL SUBJECTS von Tassano, E., Garcia, E., Obregon, R., Parras, J., Romano, A., Duarte, S., Cayre, R.

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Supplementary Material for: Clinical and Molecular Cytogenetic Characterization of a de novo Interstitial 1p31.1p31.3 Deletion in a Boy with Moderate Intellectual Disability and Se... von Tassano, E., Gamucci, A., Celle, M.E., Ronchetto, P., Cuoco, C., Gimelli, G.

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PLAG1-HAS2 fusion in lipoblastoma with masked 8q intrachromosomal rearrangement von Morerio, Cristina, Rapella, Annamaria, Rosanda, Cristina, Tassano, Elisa, Gambini, Claudio, Romagnoli, Giuseppe, Panarello, Claudio

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Differential diagnosis of congenital fibrosarcoma von Morerio, Cristina, Rapella, Annamaria, Rosanda, Cristina, Tassano, Elisa, Conte, Massimo, Gambini, Claudio, Panarello, Claudio

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L'orologio di Einstein: la riflessione filosofica sul tempo della fisica

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Loss of tubulin deglutamylase CCP1 causes infantile‐onset neurodegeneration von Shashi, Vandana, Magiera, Maria M, Klein, Dennis, Zaki, Maha, Schoch, Kelly, Rudnik‐Schöneborn, Sabine, Norman, Andrew, Lopes Abath Neto, Osorio, Dusl, Marina, Yuan, Xidi, Bartesaghi, Luca, De Marco, Patrizia, Alfares, Ahmed A, Marom, Ronit, Arold, Stefan T, Guzmán‐Vega, Francisco J, Pena, Loren DM, Smith, Edward C, Steinlin, Maja, Babiker, Mohamed OE, Mohassel, Payam, Foley, A Reghan, Donkervoort, Sandra, Kaur, Rupleen, Ghosh, Partha S, Stanley, Valentina, Musaev, Damir, Nava, Caroline, Mignot, Cyril, Keren, Boris, Scala, Marcello, Tassano, Elisa, Picco, Paolo, Doneda, Paola, Fiorillo, Chiara, Issa, Mahmoud Y, Alassiri, Ali, Alahmad, Ahmed, Gerard, Amanda, Liu, Pengfei, Yang, Yaping, Ertl‐Wagner, Birgit, Kranz, Peter G, Wentzensen, Ingrid M, Stucka, Rolf, Stong, Nicholas, Allen, Andrew S, Goldstein, David B, Schoser, Benedikt, Rösler, Kai M, Alfadhel, Majid, Capra, Valeria, Chrast, Roman, Strom, Tim M, Kamsteeg, Erik‐Jan, Bönnemann, Carsten G, Gleeson, Joseph G, Martini, Rudolf, Janke, Carsten, Senderek, Jan

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Clinical and Molecular Cytogenetic Characterization of a de novo Interstitial 1p31.1p31.3 Deletion in a Boy with Moderate Intellectual Disability and Severe Language Impairment von Tassano, Elisa, Gamucci, Alessandra, Celle, Maria E., Ronchetto, Patrizia, Cuoco, Cristina, Gimelli, Giorgio

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