Nova causa genética para defeitos do neurodesenvolvimento

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, BSc MSc PhD, Zafar, Faisal, Rana, Nuzhat, Bibi, Farah, Houlden, Henry, MD PhD, Maroofian, Reza, PhD, Person, Richard, Crunk, Amy, Savatt, Juliann M., Turner, Lisbeth, Doosti, Mohammad, PhD, Karimiani, Ehsan Ghayoor, MD MRes PhD, Saadi, Nebal Waill, Ing., Jansen, Anna C., Kros, Johan M., Verdijk, Robert, MD PhD, Jovanov-Milošević, Nataša, PhD Professor Associado, Fornerod, Maarten, Mastroberardino, Pier Giorgio, Mancini, Grazia MS.