Nueva causa genética de defectos del neurodesarrollo

Author(s): Bertoli-Avella, Aida M., MD, Al Hashem, Amal, Keren, Boris, PhD, MD, Tan, Wen-Hann, MD, Vandervore, Laura V., Schot, Rachel, Milanese, Chiara, PHD, Smits, Daphne J., Kasteleijn, Esmee, Fry, Andrew E., Pilz, Daniela T., Brock, Stefanie, Börklü-Yücel, Esra, Post, Marco, Bahi-Buisson, Nadia, MD PhD, Sánchez-Soler, María José, van Slegtenhorst, Marjon, Afenjar, Alexandra, Coury, Stephanie A., Oegema, Renske, MD, de Vries, Linda S., Fawcett, Katherine A., Nikkels, Peter GJ, Dr., Alwabel, Abdulmalik A., Tlili-Graiess, Kalthoum, Efthymiou, Stephanie, Licenciatura, Maestría y Doctorado, Zafar, Faisal, Rana, Nuzhat, Bibi, Farah, Houlden, Henry, MD PhD, Maroofian, Reza, PhD, Persona, Richard, Crunk, Amy, Savatt, Juliann M., Turner, Lisbeth, Doosti, Mohammad, PhD, Karimiani, Ehsan Ghayoor, MD MRes PhD, Saadi, Nebal Waill, Akhondian, Javad, Lequin, Maarten H., Kayserili, Hülya, Van der Spek, Peter J., Prof. Dr. Ing., Jansen, Anna C., Kros, Johan M., Verdijk, Robert, MD PhD, Jovanov-Milošević, Nataša, PhD Profesor asociado, Fornerod, Maarten, Mastroberardino, Pier Giorgio, Mancini, Grazia MS.