Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Amet Chousein"'
Autor:
Tuğçe Aksu Uzunhan, Biray Ertürk, Kürşad Aydın, Akif Ayaz, Umut Altunoğlu, Murat Hakkı Yarar, Alper Gezdirici, Dilara Füsun İçağasıoğlu, Ezgi Gökpınar İli, Bülent Uyanık, Metin Eser, Yaşar Bekir Kutbay, Yasemin Topçu, Betül Kılıç, Gonca Bektaş, Ayfer Arduç Akçay, Barış Ekici, Amet Chousein, Şahin Avcı, Atıl Yüksel, Hülya Kayserili
Publikováno v:
Clinical Neurology and Neurosurgery. 224:107560
© 2022 Elsevier B.V.Objective: Joubert syndrome is a neurodevelopmental disorder with a distinctive hindbrain malformation called molar tooth sign, causing motor and cognitive impairments. More than 40 genes have been associated with Joubert syndrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f57581bf06a2db57ba2d0c85721f96c
https://doi.org/10.1016/j.clineuro.2022.107560
https://doi.org/10.1016/j.clineuro.2022.107560
Autor:
Amet, Chousein1, Duru, Nilgün Selçuk1 nilgunduru@yahoo.com, Elevli, Murat1, Çivilibal, Mahmut1
Publikováno v:
Journal of Pediatric Research. 2015, Vol. 2 Issue 3, p118-121. 4p.