Identification and characterization of a novel chemically induced allele at the planar cell polarity gene Vangl2 von El-Hassan, Abdul-Rahman, Leung, Vicki, Kharfallah, Fares, Guyot, Marie-Claude, Allache, Redouane, Gros, Philippe, Kibar, Zoha

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A novel hypomorphic Looptail allele at the planar cell polarity Vangl2 gene von Guyot, Marie‐Claude, Bosoi, Ciprian M., Kharfallah, Fares, Reynolds, Annie, Drapeau, Pierre, Justice, Monica, Gros, Philippe, Kibar, Zoha

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Scribble1 plays an important role in the pathogenesis of neural tube defects through its mediating effect of Par-3 and Vangl1/2 localization von Kharfallah, Fares, Guyot, Marie Claude, El Hassan, Abdul Rahman, Allache, Redouane, Merello, Elisa, De Marco, Patrizia, Di Cristo, Graziella, Capra, Valeria, Kibar, Zoha

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Expression studies of Scribble 1 during anterior–posterior guidance of the commissural axons von Kharfallah, Fares, Di Crist, Graziella, Kibar, Zoha

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ISDN2014_0215: Expression studies of Scribble 1 during anterior–posterior guidance of the commissural axons von Kharfallah, Fares, Di Crist, Graziella, Kibar, Zoha

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Loss of symmetric cell division of apical neural progenitors drives DENND5A-related developmental and epileptic encephalopathy von Banks, Emily, Francis, Vincent, Lin, Sheng-Jia, Kharfallah, Fares, Fonov, Vladimir, Lévesque, Maxime, Han, Chanshuai, Kulasekaran, Gopinath, Tuznik, Marius, Bayati, Armin, Al-Khater, Reem, Alkuraya, Fowzan S., Argyriou, Loukas, Babaei, Meisam, Bahlo, Melanie, Bakhshoodeh, Behnoosh, Barr, Eileen, Bartik, Lauren, Bassiony, Mahmoud, Bertrand, Miriam, Braun, Dominique, Buchert, Rebecca, Budetta, Mauro, Cadieux-Dion, Maxime, Calame, Daniel G., Cope, Heidi, Cushing, Donna, Efthymiou, Stephanie, Elmaksoud, Marwa Abd, El Said, Huda G., Froukh, Tawfiq, Gill, Harinder K., Gleeson, Joseph G., Gogoll, Laura, Goh, Elaine S.-Y., Gowda, Vykuntaraju K., Haack, Tobias B., Hashem, Mais O., Hauser, Stefan, Hoffman, Trevor L., Hogue, Jacob S., Hosokawa, Akimoto, Houlden, Henry, Huang, Kevin, Huynh, Stephanie, Karimiani, Ehsan G., Kaulfuß, Silke, Korenke, G. Christoph, Kritzer, Amy, Lee, Hane, Lupski, James R., Marco, Elysa J., McWalter, Kirsty, Minassian, Arakel, Minassian, Berge A., Murphy, David, Neira-Fresneda, Juanita, Northrup, Hope, Nyaga, Denis M., Oehl-Jaschkowitz, Barbara, Osmond, Matthew, Person, Richard, Pehlivan, Davut, Petree, Cassidy, Sadleir, Lynette G., Saunders, Carol, Schoels, Ludger, Shashi, Vandana, Spillmann, Rebecca C., Srinivasan, Varunvenkat M., Torbati, Paria N., Tos, Tulay, Zaki, Maha S., Zhou, Dihong, Zweier, Christiane, Trempe, Jean-François, Durcan, Thomas M., Gan-Or, Ziv, Avoli, Massimo, Alves, Cesar, Varshney, Gaurav K., Maroofian, Reza, Rudko, David A., McPherson, Peter S.

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DENND5A-related developmental and epileptic encephalopathy driven by loss of symmetric cell division of apical neural progenitors von Banks, Emily, Francis, Vincent, Avoli, Massimo, Levesque, Maxime, Lin, Sheng-Jia, Varshney, Guarav, Kharfallah, Fares, Fonov, Vladimir, Rudko, David, Huang, Kevin, Petree, Cassidy, McPherson, Peter

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