Investigation of the most common clinical and imaging findings and the role of tubulin genes in the etiology of malformations of cortical development

le AKSEL KILIÇARSLAN, Özge, ATAMAN, Esra, GÜRSOY, Semra, GÜRBÜZ, Gürkan, ÜNALP, Aycan, GENÇPINAR, Pınar, OLGAÇ DÜNDAR, Nihal, EDİZER, Selvinaz, ÜLGENALP, Ayfer, GİRAY BOZKAYA, Özlem
Foilsithe in Turk J Med Sci (2020)

Identification of PCDH19 Gene Mutations/Deletions in Patients with Early Onset Epilepsy

le Gursoy, Semra, Ataman, Esra, Baysal, Bahar Toklu, Özyılmaz, Berk, Gençpınar, Pınar, Hız, Ayşe Semra, Yiş, Uluç, Ünalp, Aycan, Dündar, Nihal Olgaç, Ülgenalp, Ayfer, Erçal, Derya
Foilsithe in Ann Indian Acad Neurol (2020)

Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation

le Rohrbach, Marianne, Vandersteen, Anthony, Yiş, Uluç, Serdaroglu, Gul, Ataman, Esra, Chopra, Maya, Garcia, Sixto, Jones, Kristi, Kariminejad, Ariana, Kraenzlin, Marius, Marcelis, Carlo, Baumgartner, Matthias, Giunta, Cecilia
Foilsithe 2011

The phenotypic and molecular genetic spectrum of Alström Syndrome in 44 Turkish kindreds and a literature review of Alström Syndrome in Turkey

le Ozantürk, Ayşegül, Marshall, Jan D, Collin, Gayle B, Düzenli, Selma, Marshall, Robert P, Candan, Şükrü, Tos, Tülay, Esen, İhsan, Taşkesen, Mustafa, Çayır, Atilla, Öztürk, Şükrü, Üstün, İhsan, Ataman, Esra, Karaca, Emin, Özdemir, Taha Reşid, Erol, İlknur, Eroğlu, Fehime Kara, Torun, Deniz, Parıltay, Erhan, Yılmaz-Güleç, Elif, Karaca, Ender, Atabek, M. Emre, Elçioğlu, Nursel, Satman, İlhan, Möller, Claes, Müller, Jean, Naggert, Jürgen K, Özgül, Rıza Köksal
Foilsithe in J Hum Genet (2014)