Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm von Lindsay, Mark E, Schepers, Dorien, Bolar, Nikhita Ajit, Doyle, Jefferson J, Gallo, Elena, Fert-Bober, Justyna, Kempers, Marlies J E, Fishman, Elliot K, Chen, Yichun, Myers, Loretha, Bjeda, Djahita, Oswald, Gretchen, Elias, Abdallah F, Levy, Howard P, Anderlid, Britt-Marie, Yang, Margaret H, Bongers, Ernie M H F, Timmermans, Janneke, Braverman, Alan C, Canham, Natalie, Mortier, Geert R, Brunner, Han G, Byers, Peter H, Van Eyk, Jennifer, Van Laer, Lut, Dietz, Harry C, Loeys, Bart L

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On a conjecture of Bush and Mosteller von Van Laer, John, Van Laer, E. K.

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Indications and limits of meniscal allografts von Verdonk, R, Volpi, P, Verdonk, P, Bracht, H. Van der, Laer, M. Van, Almqvist, K.F, Eecken, S. Vander, Prospero, E, Quaglia, A

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Loss of ADAMTS19 causes progressive non-syndromic heart valve disease von Wünnemann, Florian, Ta-Shma, Asaf, Preuss, Christoph, Leclerc, Severine, van Vliet, Patrick Piet, Oneglia, Andrea, Thibeault, Maryse, Nordquist, Emily, Lincoln, Joy, Scharfenberg, Franka, Becker-Pauly, Christoph, Hofmann, Philipp, Hoff, Kirstin, Audain, Enrique, Kramer, Hans-Heiner, Makalowski, Wojciech, Nir, Amiram, Gerety, Sebastian S., Hurles, Matthew, Comes, Johanna, Fournier, Anne, Osinska, Hanna, Robins, Jeffrey, Pucéat, Michel, Elpeleg, Orly, Hitz, Marc-Phillip, Andelfinger, Gregor

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Contribution of the N-acetyltransferase 2 polymorphism NAT26A to age-related hearing impairment von Van Eyken, E, Van Camp, G, Fransen, E, Topsakal, V, Hendrickx, J J, Demeester, K, Van de Heyning, P, Mäki-Torkko, E, Hannula, S, Sorri, M, Jensen, M, Parving, A, Bille, M, Baur, M, Pfister, M, Bonaconsa, A, Mazzoli, M, Orzan, E, Espeso, A, Stephens, D, Verbruggen, K, Huyghe, J, Dhooge, I, Huygen, P, Kremer, H, Cremers, C W R J, Kunst, S, Manninen, M, Pyykkö, I, Lacava, A, Steffens, M, Wienker, T F, Van Laer, L

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Phenotypic spectrum of the SMAD3-related aneurysms–osteoarthritis syndrome von van de Laar, Ingrid M B H, van der Linde, Denise, Oei, Edwin H G, Bos, Pieter K, Bessems, Johannes H, Bierma-Zeinstra, Sita M, van Meer, Belle L, Pals, Gerard, Oldenburg, Rogier A, Bekkers, Jos A, Moelker, Adriaan, de Graaf, Bianca M, Matyas, Gabor, Frohn-Mulder, Ingrid M E, Timmermans, Janneke, Hilhorst-Hofstee, Yvonne, Cobben, Jan M, Bruggenwirth, Hennie T, van Laer, Lut, Loeys, Bart, De Backer, Julie, Coucke, Paul J, Dietz, Harry C, Willems, Patrick J, Oostra, Ben A, De Paepe, Anne, Roos-Hesselink, Jolien W, Bertoli-Avella, Aida M, Wessels, Marja W

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Clinically relevant variants in a large cohort of Indian patients with Marfan syndrome and related disorders identified by next-generation sequencing von Nayak, Shalini S., Schneeberger, Pauline E., Patil, Siddaramappa J., Arun, Karegowda M., Suresh, Pujar V., Kiran, Viralam S., Siddaiah, Sateesh, Maiya, Shreesha, Venkatachalagupta, Shrikanth K., Kausthubham, Neethukrishna, Kortüm, Fanny, Rau, Isabella, Wey-Fabrizius, Alexandra, Van Den Heuvel, Lotte, Meester, Josephina, Van Laer, Lut, Shukla, Anju, Loeys, Bart, Girisha, Katta M., Kutsche, Kerstin

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SUN-P030: The Effect of the Presence of a Clinical Pharmacist on the Nutritional Policy in an Intensive Care Unit of a General Hospital von Van Laer, E., Desmet, S., Verhelle, K.

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P01-37 The INSPIRE Initiative: using in vitro systems to predict respiratory toxicity of surfactants by pipetting and aerosol exposure von Stucki, A., Roldan, N., Sharma, M., Verstraelen, S., Jacobs, A., Hollanders, K., Van Laer, J., Remy, S., Frijns, E., Clippinger, A.J.

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Untangling a Web of Lies: Exploring Automated Detection of Deception in Computer-Mediated Communication von Ludwig, Stephan, van Laer, Tom, de Ruyter, Ko, Friedman, Mike

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A silicon-organic hybrid platform for quantum microwave-to-optical transduction von Witmer, Jeremy D, McKenna, Timothy P, Arrangoiz-Arriola, Patricio, Van Laer, Raphaël, Alex Wollack, E, Lin, Francis, Jen, Alex K-Y, Luo, Jingdong, Safavi-Naeini, Amir H

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Outcome in patients perceived as receiving excessive care across different ethical climates: a prospective study in 68 intensive care units in Europe and the USA von Benoit, D. D., Jensen, H. I., Malmgren, J., Metaxa, V., Reyners, A. K., Darmon, M., Rusinova, K., Talmor, D., Meert, A. P., Cancelliere, L., Zubek, L., Maia, P., Michalsen, A., Vanheule, S., Kompanje, E. J. O., Decruyenaere, J., Vandenberghe, S., Vansteelandt, S., Gadeyne, B., Van den Bulcke, B., Azoulay, E., Piers, R. D.

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A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment von VAN LAER, L, COUCKE, P, FRANSEN, E, ROWLAND, J, CUCCI, R. A, SMITH, R. J. H, VAN CAMP, G, MUELLER, R. F, CAETHOVEN, G, FLOTHMANN, K, PRASAD, S. D, CHAMBERLIN, G. P, HOUSEMAN, M, TAYLOR, G. R, VAN DE HEYNING, C. M

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Search for CP violation in D 0 → K S 0 K S 0 decays in proton-proton collisions at s = 13 Te V von CMS Collaboration

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P13-17 Two- and three-dimensional human cell-based in vitro systems to assess respiratory toxicity of silane vapors von Stucki, A.O., Sharma, M., Verstraelen, S., Jacobs, A., Poelmans, D., Remy, S., Maes, F., Frijns, E., Hollanders, K., Geerts, L., Voorspoels, S., Van Laer, J., Clippinger, A.J.

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A deleterious gene-by-environment interaction imposed by calcium channel blockers in Marfan syndrome von Doyle, Jefferson J, Doyle, Alexander J, Wilson, Nicole K, Habashi, Jennifer P, Bedja, Djahida, Whitworth, Ryan E, Lindsay, Mark E, Schoenhoff, Florian, Myers, Loretha, Huso, Nick, Bachir, Suha, Squires, Oliver, Rusholme, Benjamin, Ehsan, Hamid, Huso, David, Thomas, Craig J, Caulfield, Mark J, Van Eyk, Jennifer E, Judge, Daniel P, Dietz, Harry C

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Mobilization of Zn upon waterlogging riparian Spodosols is related to reductive dissolution of Fe minerals von Van Laer, L, Degryse, F, Leynen, K, Smolders, E

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Nonsyndromic hearing impairment is associated with a mutation in DFNA5 von Van Camp, Guy, Laer, Lut Van, Huizing, Egbert H, Verstreken, Margriet, Zuijlen, Diederick van, Wauters, Jan G, Bossuyt, Paul J, Van de Heyning, Paul, McGuirt, Wyman T, Smith, Richard J.H, Willems, Patrick J, Legan, P. Kevin, Richardson, Guy P

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1560 Quality of life (QoL) evaluation in head and neck cancer (HNC) patients: Electronics beats paper von Van Oevelen, K, Vanderveken, O, Dewaele, E, Verschueren, C, Mariën, S, Van Laer, C, Wouters, K, Van Fraeyenhove, B, Specenier, P

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Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment von Verhoeven, Kristien, Laer, Lut Van, Kirschhofer, Karin, Legan, P. Kevin, Hughes, David C, Schatteman, Isabelle, Verstreken, Margriet, Hauwe, Peter Van, Coucke, Paul, Chen, Achih, Smith, Richard J.H, Somers, Thomas, Offeciers, F. Erwin, Heyning, Paul Van de, Richardson, Guy P, Wachtler, Franz, Kimberling, William J, Willems, Patrick J, Govaerts, Paul J, Camp, Guy Van

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