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Balkan Medical Journal|December 29, 2018
The Incidence of Cystic Fibrosis in the Central Region of Anatolia in Turkey Between 2015 and 2016Melih Hangül, Sevgi Pekcan, Mehmet Köse, et al.Pediatric Dermatology|June 17, 2024
Four cases of Chanarin-Dorfman syndrome presenting with different types of erythrokeratodermaTubanur Çetinarslan, Havva Yazıcı, Kadri Murat Erdoğan, et al.Turkish Archives of Otorhinolaryngology|October 18, 2019
First-Line Molecular Genetic Evaluation of Autosomal Recessive Non-Syndromic Hearing LossBerk Özyılmaz, Gül Caner Mercan, Özgür Kırbıyık, et al.Turkish Journal of Urology|March 4, 2020
Evaluation of chromosomal abnormalities and Y-chromosome microdeletions in 1696 Turkish cases with primary male infertility: A single-center studyTaha Reşid Özdemir, Berk Özyılmaz, Özgür Çakmak, et al.Balkan Medical Journal|December 3, 2021
The Genetic Analysis of Cystic Fibrosis Patients With Seven Novel Mutations in the CFTR Gene in the Central Anatolian Region of TurkeyMurat Erdoğan, Mehmet Köse, Sevgi Pekcan, et al.Annals of Human Genetics|October 14, 2025
Genetic Landscape of Pediatric Dyslipidemia in a Turkish Cohort: Insights From a Single-Center ExperienceKadri Murat Erdoğan, Mehmet Berkay Akcan, Havva Yazıcı, et al.Frontiers in Oncology|February 2, 2024
Prognostic and predictive role of liquid biopsy in lung cancer patientsTuncay Goksel, Su Özgür, Aslı Tetik Vardarlı, et al.Human Mutation|June 15, 2026
Structural Variant and Repeat Expansion Findings Identified by Optical Genome Mapping in Complex Autism Spectrum Disorder With Concomitant Neurodevelopmental DisordersMehmet Burak Mutlu, Özge Beyza Gündoğdu Öğütlü, Özlem Öz, et al.Familial Cancer|June 8, 2026
Characterization of the molecular and clinical features of Multilocus Inherited Neoplasia Allelic Syndrome (MINAS) cases in the Turkish populationMehmet Berkay Akcan, Ali Duru, Kadri Murat Erdoğan, et al.The Clinical Respiratory Journal|September 27, 2020
The relation between distant metastasis and genetic change type in stage IV lung adenocarcinoma patients at diagnosisSinem Ermin, Özgür Batum, Merve Saka Güvenç, et al.Pageof 5