Reconstruction of larval origins based on genetic relatedness and biophysical modeling von Segura-García, I., Garavelli, L., Tringali, M., Matthews, T., Chérubin, L. M., Hunt, J., Box, S. J.

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Obstructive sleep apnea syndrome von Giannini, L, Garavelli, L, Mainardi, E, De Filippis, A, Esposito, L

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Expanding the clinical spectrum of the 'HDAC8-phenotype' - implications for molecular diagnostics, counseling and risk prediction von Parenti, I., Gervasini, C., Pozojevic, J., Wendt, K.S., Watrin, E., Azzollini, J., Braunholz, D., Buiting, K., Cereda, A., Engels, H., Garavelli, L., Glazar, R., Graffmann, B., Larizza, L., Lüdecke, H.J., Mariani, M., Masciadri, M., Pié, J., Ramos, F.J., Russo, S., Selicorni, A., Stefanova, M., Strom, T.M., Werner, R., Wierzba, J., Zampino, G., Gillessen-Kaesbach, G., Wieczorek, D., Kaiser, F.J.

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Prematurity, ventricular septal defect and dysmorphisms are independent predictors of pathogenic copy number variants: a retrospective study on array-CGH results and phenotypical f... von Maini, I, Ivanovski, I, Djuric, O, Caraffi, S G, Errichiello, E, Marinelli, M, Franchi, F, Bizzarri, V, Rosato, S, Pollazzon, M, Gelmini, C, Malacarne, M, Fusco, C, Gargano, G, Bernasconi, S, Zuffardi, O, Garavelli, L

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Mowat–Wilson syndrome: Facial phenotype changing with age: Study of 19 Italian patients and review of the literature von Garavelli, L., Zollino, M., Mainardi, P. Cerruti, Gurrieri, F., Rivieri, F., Soli, F., Verri, R., Albertini, E., Favaron, E., Zignani, M., Orteschi, D., Bianchi, P., Faravelli, F., Forzano, F., Seri, M., Wischmeijer, A., Turchetti, D., Pompilii, E., Gnoli, M., Cocchi, G., Mazzanti, L., Bergamaschi, R., De Brasi, D., Sperandeo, M.P., Mari, F., Uliana, V., Mostardini, R., Cecconi, M., Grasso, M, Sassi, S., Sebastio, G., Renieri, A., Silengo, M., Bernasconi, S., Wakamatsu, N., Neri, G.

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Imported dengue virus serotype 3, Yemen to Italy, 2010 von Ravanini, Paolo, Huhtamo, Eili, Hasu, Essi, Rosa, Felicita, Costantino, Stefano, Crobu, Maria G, Ilaria, Valentina, Nicosia, Anna M, Garavelli, Pietro L, Vapalahti, Olli

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Sleep in Mowat-Wilson syndrome (MWS): Clinical and polysomnografic study von Ricci, E, Di Pisa, V, Provini, F, Ubertiello, S, Bonetti, S, Ivanovski, I, Caraffi, S, Bascelli, E, Franzoni, E, Garavelli, L, Cordelli, D.M

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A short history of the initial discovery of the SHOX gene von Bernasconi, S, Garavelli, L

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Modeling the dispersal of Cape hake ichthyoplankton von GARAVELLI, L, GRÜSS, A, GROTE, B, CHANG, N, SMITH, M, VERLEY, E, STENEVIK, E. K, KAPLAN, D. M, LETT, C

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The homozygous deletion of the 3′ enhancer of the SHOX gene causes Langer mesomelic dysplasia von Bertorelli, R, Capone, L, Ambrosetti, F, Garavelli, L, Varriale, L, Mazza, V, Stanghellini, I, Percesepe, A, Forabosco, A

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Congenital Heart Defects: 15 Years of Experience of the Emilia-Romagna Registry (Italy) von Calzolari, E., Garani, G., Cocchi, G., Magnani, C., Rivieri, F., Neville, A., Astolfi, G., Baroncini, A., Garavelli, L., Gualandi, F., Scorrano, M., Bosi, G., IMER Working Group

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Intrathecal/intraventricular colistin in external ventricular device-related infections by multi-drug resistant Gram negative bacteria: case reports and review von Bargiacchi, O., Rossati, A., Car, P., Brustia, D., Brondolo, R., Rosa, F., Garavelli, P. L., De Rosa, F. G.

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Mandibuloacral dysplasia type A in childhood von Garavelli, L., D'Apice, M.R., Rivieri, F., Bertoli, M., Wischmeijer, A., Gelmini, C., De Nigris, V., Albertini, E., Rosato, S., Virdis, R., Bacchini, E., Dal Zotto, R., Banchini, G., Iughetti, L., Bernasconi, S., Superti‐Furga, A., Novelli, G.

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Oral manifestation of Goltz-Gorlin syndrome in a young girl von Callea, M, Yavuz, I, Deroma, L, Montanari, M, Clarich, G, Maglione, M, Albertini, E, Garavelli, L

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Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): Confirmation of the Mowat-Wilson syndrome von Garavelli, L., Donadio, A., Zanacca, C., Banchini, G., Della Giustina, E., Bertani, G., Albertini, G., Del Rossi, C., Rauch, A., Zweier, C., Zollino, M., Neri, G.

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22q11.2 Distal Deletion Syndrome: Description of a New Case with Truncus Arteriosus Type 2 and Review von Garavelli, L., Rosato, S., Wischmeijer, A., Gelmini, C., Esposito, A., Mazzanti, L., Franchi, F., De Crescenzo, A., Palumbo, O., Carella, M., Riccio, A.

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Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability von Grozeva, Detelina, Carss, Keren, Spasic-Boskovic, Olivera, Tejada, Maria-Isabel, Gecz, Jozef, Shaw, Marie, Corbett, Mark, Haan, Eric, Thompson, Elizabeth, Friend, Kathryn, Hussain, Zaamin, Hackett, Anna, Field, Michael, Renieri, Alessandra, Stevenson, Roger, Schwartz, Charles, Floyd, James A.B., Bentham, Jamie, Cosgrove, Catherine, Keavney, Bernard, Bhattacharya, Shoumo, Hurles, Matthew, Raymond, F. Lucy

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Blue crab larval dispersal highlights population connectivity and implications for fishery management von Criales, Maria M., Chérubin, Laurent, Gandy, Ryan, Garavelli, Lysel, Ghannami, Mohamed Ali, Crowley, Claire

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Clinical and molecular characterization of 40 patients with classic Ehlers-Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutations von Ritelli, Marco, Dordoni, Chiara, Venturini, Marina, Chiarelli, Nicola, Quinzani, Stefano, Traversa, Michele, Zoppi, Nicoletta, Vascellaro, Annalisa, Wischmeijer, Anita, Manfredini, Emanuela, Garavelli, Livia, Calzavara-Pinton, Piergiacomo, Colombi, Marina

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Charge degeneracy for a Thomas–Fermi hydrogen molecule: Bound–unbound transition von Diniz, João B., Penna, André L.A., Garavelli, Sérgio L., Oliveira, Fernando A.

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