Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Yaşar Bekir KUTBAY"'
Autor:
Özge Köprülü, Sezer Acar, Kadri Murat Erdoğan, Özlem Nalbantoğlu, Tarık Kırkgöz, Gülçin Arslan, Beyhan Özkaya, Yaşar Bekir Kutbay, Behzat Özkan
Publikováno v:
Journal of Pediatric Research, Vol 9, Iss 4, Pp 401-408 (2022)
The 45,X/47,XYY mosaicism is an extremely rare genetic disorder with highly phenotypic manifestations such as ovotesticular disorders of sexual development, mixed gonadal dysgenesis and Turner syndrome. Herein, we report two cases with very distincti
Externí odkaz:
https://doaj.org/article/ac925d37e44443fb9c358adf8d8c2b2a
Autor:
Berk Özyılmaz, Gül Caner Mercan, Özgür Kırbıyık, Taha Reşid Özdemir, Samira Özkara, Özge Özer Kaya, Yaşar Bekir Kutbay, Kadri Murat Erdoğan, Merve Saka Güvenç, Altuğ Koç
Publikováno v:
Turkish Archives of Otorhinolaryngology, Vol 57, Iss 3, Pp 140-148 (2019)
Objective:The aim of this study is to investigate the efficiency of a first-line molecular genetic evaluation approach, in children with deafness.Methods:Patients who were found to have sensorineural hearing loss by age-appropriate audiological tests
Externí odkaz:
https://doaj.org/article/66a97428e8c94324ac5de34e16d365bb
Publikováno v:
Turkish Journal of Hematology, Vol 34, Iss 2, Pp 197-199 (2017)
Externí odkaz:
https://doaj.org/article/c6d3d28405194af78e7e28e0b1ce6541
Autor:
Tuba Demirci Yıldırım, Utku Erdem Soyaltın, Altuğ Koç, Serkan Yıldız, Mehmet Tanrısev, Yaşar Bekir Kutbay, Ferhat Ekinci, Süleyman Yıldırım, Harun Akar, Cengiz Ceylan
Publikováno v:
The Journal of Tepecik Education and Research Hospital. 33:45-49
Autor:
Alper İLERİ, Suna YILDIRIM KARACA, Hande İLERİ, Hakan GÖLBAŞI, Alkım Gülşah ŞAHİNGÖZ YILDIRIM, Yaşar Bekir KUTBAY, Altuğ KOÇ, Mehmet ÖZEREN
Objective: Non-invasive prenatal testing (NIPT) and fetal fraction (FF) are shown to be affected by various factors like maternal characteristics or medications. Recently medications are now undergoing evaluation as influencing factors. Still no data
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e88b8010a3634769ade2d0ce3892bccc
https://hdl.handle.net/11454/78947
https://hdl.handle.net/11454/78947
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
Autor:
Burak, Bayraktar, Ebru Şahin, Güleç, Yaşar Bekir, Kutbay, Can, Köse, Esra Bahar, Gür, Ahmet, Demir
Publikováno v:
Journal of human reproductive sciences. 15(1)
Follicle-stimulating hormone (FSH) plays a key role in fertility and shows its effect through the FSH receptor (FSHR), which is localized in cells.The aim of this study was to examine pregnancy outcomes and responses to controlled ovarian stimulation
Publikováno v:
Journal of Human Reproductive Sciences, Vol 15, Iss 1, Pp 58-63 (2022)
Background: Follicle-stimulating hormone (FSH) plays a key role in fertility and shows its effect through the FSH receptor (FSHR), which is localized in cells. Aims: The aim of this study was to examine pregnancy outcomes and responses to controlled
Externí odkaz:
https://doaj.org/article/52ab4afe38294582936c3379931e323e