First-trimester euploid miscarriages analysed by array-CGH by Viaggi, Chiara Donatella, Cavani, S, Malacarne, M, Floriddia, F, Zerega, G, Baldo, C, Mogni, M, Castagnetta, M, Piombo, G, Coviello, D. A, Camandona, F, Lijoi, D, Insegno, W, Traversa, M, Pierluigi, M

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Clinical and molecular characterisation of 80 patients with 5p deletion: genotype-phenotype correlation by Mainardi, P Cerruti, Perfumo, C, Calì, A, Coucourde, G, Pastore, G, Cavani, S, Zara, F, Overhauser, J, Pierluigi, M, Bricarelli, F Dagna

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Array‐CGH and clinical characterization in a patient with subtelomeric 6p deletion without ocular dysgenesis by Piccione, Maria, Antona, R., Salzano, E., Cavani, S., Malacarne, M., Morreale Bubella, R., Pierluigi, M., Viaggi, C.D., Corsello, Giovanni

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Frequency of hyper-, hypohaploidy and diploidy in ejaculate, epididymal and testicular germ cells of infertile patients by Bernardini, L., Gianaroli, L., Fortini, D., Conte, N., Magli, C., Cavani, S., Gaggero, G., Tindiglia, C., Ragni, N., Venturini, P.L.

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Mutation analysis of the NSD1 gene in a group of 59 patients with congenital overgrowth by Cecconi, M., Forzano, F., Milani, D., Cavani, S., Baldo, C., Selicorni, A., Pantaleoni, C., Silengo, M., Ferrero, G.B., Scarano, G., Della Monica, M., Fischetto, R., Grammatico, P., Majore, S., Zampino, G., Memo, L., Cordisco, E. Lucci, Neri, G., Pierluigi, M., Bricarelli, F. Dagna, Grasso, M., Faravelli, Francesca

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Prenatal diagnosis of Gollop-Wolfgang Complex by Forzano, Francesca, Viassolo, V., Castagnetta, M., Cavani, S., Battistuzzi, L., Garbati, E., Emiliozzi, M.C., Cecchi, A., Faravelli, F., Lituania, M.

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Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology by De Rocco, Daniela, Bottega, Roberta, Cappelli, Enrico, Cavani, Simona, Criscuolo, Maria, Nicchia, Elena, Corsolini, Fabio, Greco, Chiara, Borriello, Adriana, Svahn, Johanna, Pillon, Marta, Mecucci, Cristina, Casazza, Gabriella, Verzegnassi, Federico, Cugno, Chiara, Locasciulli, Anna, Farruggia, Piero, Longoni, Daniela, Ramenghi, Ugo, Barberi, Walter, Tucci, Fabio, Perrotta, Silverio, Grammatico, Paola, Hanenberg, Helmut, Della Ragione, Fulvio, Dufour, Carlo, Savoia, Anna

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Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal survey by Sensi, A., Cavani, S., Villa, N., Pomponi, M. G., Fogli, A., Gualandi, F., Grasso, M., Sala, E., Pietrobono, R., Baldinotti, F., Savin, E., Ferlini, A., Cecconi, M., Rossi, S., Gallone, S., Bellini, C., Neri, G., Martinoli, E., Simi, P., Dalprà, L., Genuardi, M., Dagna-Bricarelli, F., Calzolari, E.

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The first three mosaic cri du chat syndrome patients with two rearranged cell lines by PERFUMO, C, MAINARDI, P CERRUTI, CALÌ, A, COUCOURDE, G, ZARA, F, CAVANI, S, OVERHAUSER, J, BRICARELLI, F DAGNA, PIERLUIGI, M

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Cryptic 1p36.3/6q25.2 translocation in three generations ascertained through a foetus with IUGR and cerebral malformations by Cavani, S., Perfumo, C., Faravelli, F., Malacarne, M., Sogliani, M., Piombo, G., Zerega, G., Zucca, M., Dagna Bricarelli, F., Pierluigi, M.

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Acquired mutations in GATA1 in neonates with Down's syndrome with transient myeloid disorder by Groet, Jürgen, McElwaine, Suzanne, Spinelli, Monica, Rinaldi, Andrea, Burtscher, Ingo, Mulligan, Claire, Mensah, Afua, Cavani, Simona, Dagna-Bricarelli, Franca, Basso, Giuseppe, Cotter, Finbarr E, Nizetic, Dean

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Lack of evidence of a genetic origin in the impaired spermatogenesis of a patient cohort with low-grade varicocele by Foppiani, L, Cavani, S, Piredda, S, Perroni, L, Fazzuoli, L, Giusti, M

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18q‐ syndrome and ectodermal dysplasia syndrome: Description of a child and his family by Zannolli, R., Pierluigi, M., Pucci, L., Lagrasta, N., Gasparre, O., Matera, M.R., Di Bartolo, R.M., Mazzei, M.A., Sacco, P., Miracco, C., de Santi, M.M., Aitiani, P., Cavani, S., Pellegrini, L., Fimiani, M., Alessandrini, C., Galluzzi, P., Livi, W., Gonnelli, S., Terrosi‐Vagnoli, P., Zappella, M., Morgese, G.

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Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology by De Rocco, D., Bottega, R., Cappelli, E., Cavani, S., Criscuolo, M., Nicchia, E., Corsolini, F., Greco, C., Borriello, A., Svahn, J., Pillon, M., Mecucci, C., Casazza, G., Verzegnassi, F., Cugno, C., Locasciulli, A., Farruggia, P., Longoni, D., Ramenghi, U., Barberi, W., Tucci, F., Perrotta, S., Grammatico, P., Hanenberg, H., Ragione, F. D., Dufour, C., Savoia, A.

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Novel CNS syndrome and ectodermal dysplasia by Zannolli, R., Macucci, F., Di Bartolo, R.M., Serracca, L., Miracco, C., de Santi, M.M., Giannini, F., Malandrini, A., Galluzzi, P., De Robertis, S., Hadjistilianou, T., Perotti, R., Fimiani, M., Doldo, T., Giorgetti, R., Cavani, S., Pierluigi, M.

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Microarray transcript profiling distinguishes the transient from the acute type of megakaryoblastic leukaemia (M7) in Down's syndrome, revealing PRAME as a specific discriminating... by McElwaine, Suzanne, Mulligan, Claire, Groet, Jürgen, Spinelli, Monica, Rinaldi, Andrea, Denyer, Gareth, Mensah, Afua, Cavani, Simona, Baldo, Chiara, Dagna‐Bricarelli, Franca, Hann, Ian, Basso, Giuseppe, Cotter, Finbarr E., Nizetic, Dean

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Metabolic disorders across hepatocellular carcinoma in Italy by Morisco, Filomena, Guarino, Maria, Valvano, Maria R., Auriemma, Francesco, Farinati, Fabio, Giannini, Edoardo G., Ciccarese, Francesca, Tovoli, Francesco, Rapaccini, Gian Ludovico, Di Marco, Maria, Caturelli, Eugenio, Zoli, Marco, Borzio, Franco, Sacco, Rodolfo, Cabibbo, Giuseppe, Felder, Martina, Benvengù, Luisa, Gasbarrini, Antonio, Svegliati Baroni, Gianluca, Foschi, Francesco G., Biasini, Elisabetta, Masotto, Alberto, Virdone, Roberto, Marra, Fabio, Caporaso, Nicola, Trevisani, Franco, Sessa, Anna, Marafatto, Filippo, Peserico, Giulia, Pozzan, Caterina, Brunacci, Matteo, Moscatelli, Alessandro, Pellegatta, Gaia, Savarino, Vincenzo, Del Poggio, Paolo, Olmi, Stefano, Matthaeis, Nicoletta, Balsamo, Claudia, Vavassori, Elena, Roselli, Paola, Lauria, Valentina, Pelecca, Giorgio, Mismas, Valeria, Rossi, Margherita, Attardo, Simona, Cavani, Giulia, Mega, Andrea, Rinninella, Emanuele, Ortolani, Alessio, Bevilacqua, Vittoria, Chiara Dall'Aglio, Anna, Ercolani, Giorgio, Fiorini, Erica, Casadei Gardini, Andrea, Lanzi, Arianna, Mirici Cappa, Federica, Missale, Gabriele, Porro, Emanuela, Marchetti, Fabiana, Valerio, Matteo, Affronti, Andrea, Orlando, Emanuele, Rosa Barcellona, Maria, Aburas, Sami, Dragoni, Gabriele, Campani, Claudia, Biselli, Maurizio, Bucci, Laura, Caraceni, Paolo, Cucchetti, Alessandro, Domenicali, Marco, Garuti, Francesca, Gramenzi, Annagiulia, Magalotti, Donatella, Serra, Carla, Granito, Alessandro, Negrini, Giulia, Napoli, Lucia, Piscaglia, Fabio

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Mathematical modeling of arterial pressure response to hemodialysis-induced hypovolemia by Cavalcanti, Silvio, Cavani, Silvia, Ciandrini, Andrea, Avanzolini, Guido

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Bruising: A Neglected, Though Patient-Relevant Complication of Insulin Injections Coming to Light from a Real-Life Nationwide Survey by Gentile, Sandro, Guarino, Giuseppina, Della Corte, Teresa, Marino, Giampiero, Satta, Ersilia, Romano, Carmine, Alfrone, Carmelo, lmberti, Clelia, Strollo, Felice

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Mild Generalized Epilepsy and Developmental Disorder Associated with Large Inv Dup(15) by Chifari, Rosanna, Guerrini, Renzo, Pierluigi, Mauro, Cavani, Simona, Sgrò, Vincenzo, Elia, Maurizio, Canger, Raffaele, Canevini, Maria Paola

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