Metabarcoding for the authentication of complex seafood products: The fish burger case von Giusti, A., Malloggi, C., Lonzi, V., Forzano, R., Meneghetti, B., Solimeo, Antonio, Tinacci, L., Armani, A.

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Building façade integrated solar thermal collectors for air heating: experimentation, modelling and applications von Agathokleous, R., Barone, G., Buonomano, A., Forzano, C., Kalogirou, S.A., Palombo, A.

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Development and validation of a new TRNSYS Type for thermosiphon flat-plate solar thermal collectors: energy and economic optimization for hot water production in different climate... von Kalogirou, S.A., Agathokleous, R., Barone, G., Buonomano, A., Forzano, C., Palombo, A.

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Building integration of active solar energy systems: A review of geometrical and architectural characteristics von Vassiliades, C., Agathokleous, R., Barone, G., Forzano, C., Giuzio, G.F., Palombo, A., Buonomano, A., Kalogirou, S.

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Regulating the communication of genetic risk information: the Italian legal approach to questions of confidentiality and disclosure von Battistuzzi, L, Ciliberti, R, Forzano, F, De Stefano, F

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Fine-grained facial phenotype–genotype analysis in Wolf–Hirschhorn syndrome von Hammond, Peter, Hannes, Femke, Suttie, Michael, Devriendt, Koen, Vermeesch, Joris Robert, Faravelli, Francesca, Forzano, Francesca, Parekh, Susan, Williams, Steve, McMullan, Dominic, South, Sarah T, Carey, John C, Quarrell, Oliver

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A specific mutation in TBL1XR1 causes Pierpont syndrome von Heinen, Charlotte A, Jongejan, Aldo, Watson, Peter J, Redeker, Bert, Boelen, Anita, Boudzovitch-Surovtseva, Olga, Forzano, Francesca, Hordijk, Roel, Kelley, Richard, Olney, Ann H, Pierpont, Mary Ella, Schaefer, G Bradley, Stewart, Fiona, van Trotsenburg, A S Paul, Fliers, Eric, Schwabe, John W R, Hennekam, Raoul C

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Self-Control and Impulsivity in Children: Multiple Behavioral Measures von Forzano, L. B., Michels, Jennifer L., Carapella, R. K., Conway, Patrick, Chelonis, J. J.

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Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes... von Vega, H, Trainer, A H, Gordillo, M, Crosier, M, Kayserili, H, Skovby, F, Uzielli, M L Giovannucci, Schnur, R E, Manouvrier, S, Blair, E, Hurst, J A, Forzano, F, Meins, M, Simola, K O J, Raas-Rothschild, A, Hennekam, R C M, Jabs, E Wang

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Integrated electrodes and electrospray emitter for polymer microfluidic nanospray-MS interface von Forzano, Anna V, Becirovic, Vedada, Martin, R. Scott, Edwards, James 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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259th ENMC international workshop: Anaesthesia and neuromuscular disorders 11 December, 2020 and 28–29 May, 2021 von van den Bersselaar, LR, Riazi, S, Snoeck, MMJ, Jungbluth, H, Voermans, NC, Bastian, Börge, van den Bersselaar, Luuk R., Cornel, Martina, Cambronero, Oscar Díaz, Dietrich, Klaus, van Esch, Charlotte, Forzano, Francesca, Gillies, Robyn, Hellblom, Anna, Heytens, Luc, Hopkins, Phil, Johannsen, Stephan, Jungbluth, Heinz, Kamsteeg, Erik-Jan, Klein, Andrea, Litman, Ron, Løkken, Nicoline, Münster, Tino, Reimann, Jens, Rendu, John, Riazi, Sheila, Rueffert, Henrik, Silva, Helga CA, Snoeck, Marc MJ, Soller, Maria, Stowell, Kathryn, Tasca, Giorgio, Veyckemans, Francis, Vilchez, Juan Jesus, Voermans, Nicol C.

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Craniofacial characteristics of fragile X syndrome in mouse and man von Heulens, Inge, Suttie, Michael, Postnov, Andrei, De Clerck, Nora, Perrotta, Concetta S, Mattina, Teresa, Faravelli, Francesca, Forzano, Francesca, Kooy, R Frank, Hammond, Peter

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Developmental trajectories of neuroanatomical alterations associated with the 16p11.2 Copy Number Variations von Cárdenas-de-la-Parra, Alonso, Martin-Brevet, Sandra, Moreau, Clara, Rodriguez-Herreros, Borja, Fonov, Vladimir S., Maillard, Anne M., Zürcher, Nicole R., Addor, Marie-Claude, Andrieux, Joris, Arveiler, Benoît, Baujatm, Geneviève, Sloan-Bénan, Frédérique, Belfiore, Marco, Bonneau, Dominique, Bouquillon, Sonia, Boute, Odile, Brusco, Alfredo, Busa, Tiffany, Caberg, Jean-Hubert, Campion, Dominique, Colombert, Vanessa, Cordier, Marie-Pierre, David, Albert, Debray, François-Guillaume, Delrue, Marie-Ange, Doco-Fenzy, Martine, Dunkhase-Heinl, Ulrike, Edery, Patrick, Fagerberg, Christina, Faivre, Laurence, Forzano, Francesca, Genevieve, David, Gérard, Marion, Giachino, Daniela, Guichet, Agnès, Guillin, Olivier, Héron, Delphine, Isidor, Bertrand, Jacquette, Aurélia, Jaillard, Sylvie, Journel, Hubert, Keren, Boris, Lacombe, Didier, Lebon, Sébastien, Le Caignec, Cédric, Lemaître, Marie-Pierre, Lespinasse, James, Mathieu-Dramart, Michèle, Mercier, Sandra, Mignot, Cyril, Missirian, Chantal, Petit, Florence, Pilekær Sørensen, Kristina, Pinson, Lucile, Plessis, Ghislaine, Prieur, Fabienne, Rooryck-Thambo, Caroline, Rossi, Massimiliano, Sanlaville, Damien, Schlott Kristiansen, Britta, Schluth-Bolard, Caroline, Till, Marianne, Van Haelst, Mieke, Van Maldergem, Lionel, Hadjikhani, Nouchine, Beckmann, Jacques S., Reymond, Alexandre, Draganski, Bogdan, Jacquemont, Sébastien, Collins, D. Louis

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Molecular characterization of Italian nevoid basal cell carcinoma syndrome patients von Pastorino, L., Cusano, R., Nasti, S., Faravelli, F., Forzano, F., Baldo, C., Barile, M., Gliori, S., Muggianu, M., Ghigliotti, G., Lacaita, M.G., Lo Muzio, L., Bianchi-Scarra, G.

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Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities von D'Angelo, Debra, Lebon, Sébastien, Chen, Qixuan, Martin-Brevet, Sandra, Snyder, LeeAnne Green, Hippolyte, Loyse, Hanson, Ellen, Maillard, Anne M, Faucett, W Andrew, Macé, Aurélien, Pain, Aurélie, Bernier, Raphael, Chawner, Samuel J R A, David, Albert, Andrieux, Joris, Aylward, Elizabeth, Baujat, Genevieve, Caldeira, Ines, Conus, Philippe, Ferrari, Carrina, Forzano, Francesca, Gérard, Marion, Goin-Kochel, Robin P, Grant, Ellen, Hunter, Jill V, Isidor, Bertrand, Jacquette, Aurélia, Jønch, Aia E, Keren, Boris, Lacombe, Didier

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Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth von Douglas, Jenny, Cilliers, Deirdre, Coleman, Kim, Tatton-Brown, Katrina, Barker, Karen, Bernhard, Brigitte, Burn, John, Huson, Susan, Josifova, Dragana, Lacombe, Didier, Malik, Mohsin, Mansour, Sahar, Reid, Evan, Cormier-Daire, Valerie, Cole, Trevor, Childhood Overgrowth Collaboration, The, Rahman, Nazneen

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Mutation analysis of the NSD1 gene in a group of 59 patients with congenital overgrowth von 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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Uncommon association of germline mutations of RET proto-oncogene and CDKN2A gene von Foppiani, L, Forzano, F, Ceccherini, I, Bruno, W, Ghiorzo, P, Caroli, F, Quilici, P, Bandelloni, R, Arlandini, A, Sartini, G, Cabria, M, Del Monte, P

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Assignment of a new congenital fibrosis of extraocular muscles type 3 (CFEOM3) locus, FEOM4, based on a balanced translocation t(2;13) (q37.3;q12.11) and identification of candidat... von Aubourg, P, Krahn, M, Bernard, R, Nguyen, K, Forzano, O, Boccaccio, I, Delague, V, De Sandre-Giovannoli, A, Pouget, J, Depétris, D, Mattei, M-G, Philip, N, Lévy, N

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