Maternal uniparental disomy of chromosome 16 [upd(16)mat]: clinical features are rather caused by (hidden) trisomy 16 mosaicism than by upd(16)mat itself by Scheuvens, R., Begemann, M., Soellner, L., Meschede, D., Raabe‐Meyer, G., Elbracht, M., Schubert, R., Eggermann, T.

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OP02.10: Non‐invasive prenatal detection of fetal autosomal aneuploidies using massively parallel sequencing: a collaborative study in Europe by Hofmann, W., Stumm, M., Haug, K., Blank, C., Wüstemann, M., Schulze, B., Raabe‐Meyer, G., Hempel, M., Schelling, M., Ostermayer, E., Langer‐Freitag, S., Burkhardt, T., Zimmermann, R., Beck, M., Schleicher, T., Kumar, Y., Schöner, D., Grömminger, S., Entezami, M.

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POSTER VIEWING SESSION - REPRODUCTIVE (EPI) GENETICS by Acar-Perk, B., Salmassi, A., Arnold, N., Schmutzler, A. G., Thornhill, A. R., Montjean, D., McElreavey, K., Yilmaz, A., Dahan, M., Tan, S. L., Skakkebaek, N. E., Toppari, J., Gianaroli, L., Koscinski, I., Kuentz, P., Velez de la Calle, J., Carre-Pigeon, F., Barratt, C., Castelletti, E., Pepas, L., Braude, P., El-Toukhy, T., Bouraima, H., Goverde, A. J., Piomboni, P., Ota, S., Inagaki, A., Egusa, H., Nakanishi, I., Yanagihara, I., Alvaro Mercadal, B., Lopez-Teijon, M., Fernandez, S., Ito, Y., Zeiss, C., Demir, R., Ku, S. Y., Park, K. E., Choi, Y. M., Moon, S. Y., Linan, A., Palomares, A. R., Perez-Nevot, B., Ruiz Martin, A., Ruiz Galdon, M., Tao, X., Ferry, K. M., Neelima, C. H., Sravanthi, D., Sreelakshmi, K. S., Deepti, H., Steegers, E. A. P., Galjaard, R. J., van den Berg, I. M., Spizzichino, L., Biricik, A., Rienzi, L., Pantos, K., Metspalu, A., Salumets, A., Cervero, A., Mercader, A., Vidal, C., Pellicer, A., Mozdarani, H., Moghbeli Nejad, S., Ibala-Romdhane, S., Ajina, M., Martinez, M. C., Milan, M., Delgado, A., Amorocho, B., Petrussa, L., De Munck, N., De Rycke, M., Martinez-Conejero, J. A., Horcajadas, J. A., Raabe-Meyer, G., Zimmer, J., Sugawara, N., Manome, T., Nagai, R., Georgiou, I., Lazaros, L., Xita, N., Hatzi, E., Benner, A., Du, L., Kearns, W. G., Shen, X., Zeng, Y., Zhuang, G., Richter, K., Andreeva, P., Shterev, A., Turley, H., Immesberger, A., Haaf, T., Schorsch, M., Golan, N.

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Cat eye syndrome: Clinical, cytogenetics and familial findings in a large cohort of 43 patients highlighting the importance of congenital heart disease and inherited cases by Jedraszak, Guillaume, Jobic, Florence, Receveur, Aline, Bilan, Frédéric, Gilbert‐Dussardier, Brigitte, Tiffany, Busa, Missirian, Chantal, Willems, Marjolaine, Odent, Sylvie, Lucas, Josette, Dubourg, Christele, Schaefer, Elise, Scheidecker, Sophie, Lespinasse, James, Goldenberg, Alice, Guerrot, Anne‐Marie, Joly‐Helas, Géraldine, Chambon, Pascal, Le Caignec, Cédric, David, Albert, Coutton, Charles, Satre, Véronique, Vieville, Gaëlle, Amblard, Florence, Harbuz, Radu, Sanlaville, Damien, Till, Marianne, Vincent‐Delorme, Catherine, Colson, Cindy, Andrieux, Joris, Naudion, Sophie, Toutain, Jérome, Rooryck, Caroline, Fréminville, Bénédicte, Prieur, Fabienne, Daire, Valérie Cormier, Amram, Daniel, Kleinfinger, Pascale, Schulze, Matthias B., Raabe‐Meyer, Gisela, Courage, Carolina, Lemke, Johannes, Stefanou, Eunice G., Loretta, Thomaidis, Emmanouil, Manolakos, Tzeli, Sophia Kitsiou, Sodowska, Henryka, Anderson, Jasen, Nandini, Adayapalam, Copin, Henri, Garçon, Loïc, Liehr, Thomas, Morin, Gilles

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