Novel mutations with clinical variability and surgical experience in van der woude syndrome by Ahmet Cevdet Ceylan, Figen Ozgur, Ibrahim Vargel

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The Relationship Between Methylation Defects and Different Genetic Disorders: Two Case Reports by Emine Aydın, Ahmet Cevdet Ceylan, Mehmet Sinan Beksaç

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Case Reports of Patients Diagnosed with Familial Hypocalciuric Hypercalcemia, A Disorder That Should be Kept in Mind in Hypercalcemia Cases by Ayşe Derya Buluş, Yüksel Yaşartekin, Ahmet Cevdet Ceylan

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Sertoli-Leydig cell tumor, thyroid follicular carcinoma and rhabdomyosarcoma of the uterine cervix in a prepubertal girl with pathogenic germline variant in DICER1 gene by İbrahim Karnak, Ahmet Cevdet Ceylan, Mithat Haliloğlu, Alev Özön, Diclehan Orhan, Tezer Kutluk

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A novel homozygous mutation in the USP53 gene as the cause of benign recurrent intrahepatic cholestasis in children: a case report by Burcu Berberoğlu Ateş, Ahmet Cevdet Ceylan, Gülin Hızal, Fatih Duran, Hayriye Tatlı Doğan, Şamil Hızlı

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Importance and usage of chromosomal microarray analysis in diagnosing intellectual disability, global developmental delay, and autism; and discovering new loci for these disorders by Ahmet Cevdet Ceylan, Senol Citli, Haktan Bagis Erdem, Ibrahim Sahin, Elif Acar Arslan, Murat Erdogan

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Determinación de los polimorfismos rs2058265, rs6464214 y rs7456421 de la proteína cinasa 2 que interactúan con el homeodominio en pacientes con cálculos renales by Cavit Ceylan, Omer Gokhan-Doluoglu, Sedat Taştemur, Ibrahim Keleş, Gulay Ceylan, Ahmet Cevdet-Ceylan, Emre Uzun, Eda Tokat

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