Browsing by Subject 17q21.31 Microdeletion Syndrome

Showing results 1 to 1 of 1
Issue DateTitleAuthor(s)
2023The clinical phenotype of Koolen-de Vries syndrome in Turkish patients and literature reviewKaramık, Gökçen; Tüysüz, Beyhan; Işık, Esra; Yılmaz, Ayşegül ; Alanay, Yasemin; Çiftçi Sunamak, Evrim; Durmusalioglu, Enise Avcı; Ozkinay, Ferda; Cetin, Gokhan Ozan ; Ozturk, Nuray; Mihci, Ercan