Ground deformation reveals the scale-invariant conduit dynamics driving explosive basaltic eruptions von Ripepe, M., Lacanna, G., Pistolesi, M., Silengo, M. C., Aiuppa, A., Laiolo, M., Massimetti, F., Innocenti, L., Della Schiava, M., Bitetto, M., La Monica, F. P., Nishimura, T., Rosi, M., Mangione, D., Ricciardi, A., Genco, R., Coppola, D., Marchetti, E., Delle Donne, D.

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Fetal growth patterns in Beckwith-Wiedemann syndrome von Mussa, A., Russo, S., de Crescenzo, A., Freschi, A., Calzari, L., Maitz, S., Macchiaiolo, M., Molinatto, C., Baldassarre, G., Mariani, M., Tarani, L., Bedeschi, M.F., Milani, D., Melis, D., Bartuli, A., Cubellis, M.V., Selicorni, A., Silengo, M.C., Larizza, L., Riccio, A., Ferrero, G.B.

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MLL2 mutation detection in 86 patients with Kabuki syndrome: a genotype-phenotype study von Makrythanasis, P, van Bon, BW, Steehouwer, M, Rodríguez-Santiago, B, Simpson, M, Dias, P, Anderlid, BM, Arts, P, Bhat, M, Augello, B, Biamino, E, Bongers, EMHF, del Campo, M, Cordeiro, I, Cueto-González, AM, Cuscó, I, Deshpande, C, Frysira, E, Izatt, L, Flores, R, Galán, E, Gener, B, Gilissen, C, Granneman, SM, Hoyer, J, Yntema, HG, Kets, CM, Koolen, DA, Marcelis, CL, Medeira, A, Micale, L, Mohammed, S, de Munnik, SA, Nordgren, A, Psoni, S, Reardon, W, Revencu, N, Roscioli, T, Ruiterkamp-Versteeg, M, Santos, HG, Schoumans, J, Schuurs-Hoeijmakers, JHM, Silengo, MC, Toledo, L, Vendrell, T, van der Burgt, I, van Lier, B, Zweier, C, Reymond, A, Trembath, RC, Perez-Jurado, L, Dupont, J, de Vries, BBA, Brunner, HG, Veltman, JA, Merla, G, Antonarakis, SE, Hoischen, A

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Preliminary seismic microzonation in a mountainmunicipality of Tuscany (Italy) von Matassoni, L., Fiaschi, A., Silengo, M. C., Lotti, A., Saccorotti, G.

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Total Anonychia congenita in a Woman with Normal Intelligence: Report of a Further Case von Priolo, M., Rosaia, L., Seri, M., Silengo, M.C., Ravazzolo, R., Lerone, M.

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Prevalence of beckwith-wiedemann syndrome in North West of Italy von Mussa, Alessandro, Russo, Silvia, De Crescenzo, Agostina, Chiesa, Nicoletta, Molinatto, Cristina, Selicorni, Angelo, Richiardi, Lorenzo, Larizza, Lidia, Silengo, Margherita Cirillo, Riccio, Andrea, Ferrero, Giovanni Battista

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A novel H208D TP63 mutation in a familial case of ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome without clefting von Sorasio, L., Biamino, E., Garelli, E., Ferrero, G. B., Silengo, M. C.

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Seismo-acoustic energy partitioning of a powder snow avalanche von Marchetti, Emanuele, van Herwijnen, Alec, Christen, Marc, Silengo, Maria Cristina, Barfucci, Giulia

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Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome von Riccio, Andrea, Sparago, Angela, Cerrato, Flavia, Vernucci, Maria, Ferrero, Giovanni Battista, Silengo, Margherita Cirillo

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Multiple sutural synostosis and congenital cataracts von LERONE, M, ROMEO, G, CONRAD, E, SILVANO, S, CAMA, A, SILENGO, C. M

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A novel H208D TP63 mutation in a familial case of ectrodactyly–ectodermal dysplasia–cleft lip/palate syndrome without clefting von Sorasio, L., Biamino, E., Garelli, E., Ferrero, G. B., Silengo, M. C.

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A new syndrome with cerebro-oculo-skeletal-renal involvement von Silengo, M C, Lerone, M, Pelizza, A, Gatti, R, Barabino, A, Romeo, G

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Congenital diaphragmatic hernia associated with ipsilateral upper limb reduction defects: Report of a case with thumb hypoplasia von Lerone, M., Soliani, M., Corea, D., Romeo, G., Martucciello, G., Silengo, M. C.

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Congenital hypoplastic anaemia in a patient with a new multiple congenital anomalies-mental retardation syndrome von Mori, Pier Giorgio, Priolo, Manuela, Lerone, Margherita, Pasino, Mirella, Caroli, Francesco, Cusano, Roberto, Seri, Marco, Silengo, Margherita Cirillo

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Pierre Robin syndrome with hyperphalangism-clinodactylysm of the index finger: a possible new palato-digital syndrome von Silengo, M C, Franceschini, P, Cerutti, A, Fabris, C

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Ectodermal abnormalities in Kabuki syndrome von Lerone, Margherita, Priolo, Manuela, Naselli, Arturo, Vignolo, Marina, Romeo, Giovanni, Silengo, Margherita Cirillo

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Unilateral radio-ulnar synostosis associated with hypotonia, developmental delay, and facial dysmorphism von Divizia, Maria Teresa, Baban, Anwar, Pessagno, Alice, Boero, Silvio, Ravazzolo, Roberto, Silengo, Margherita Cirillo, Lerone, Margherita

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Extra band in the 9qh+ chromosome in a normal father and in his child with multiple congenital anomalies von Silengo, M C, Davi, G F, Franceschini, P

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Radiological features in trisomy 8 von Silengo, M C, Davi, G F, Franceschini, P

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How wide is the ocular spectrum of Delleman syndrome? von Divizia, Maria Teresa, Priolo, Manuela, Priolo, Enrico, Ottonello, Giancarlo, Baban, Anwar, Rossi, Andrea, Silengo, Margherita Cirillo, Lerone, Margherita

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