Showing results (1-10 of 20) with videos related to
Sort By:
Pageof 2
Journal of Pediatric Genetics|November 17, 2017
A Rare Double Aneuploidy Case (Down-Klinefelter)Sevcan Tug Bozdogan, Atil BisginJournal of Pediatric Genetics|May 9, 2024
A Novel Mutation Diagnosing in Allan-Herndon-Dudley's SyndromeRojan Ipek, Sevcan Tug Bozdogan, Mustafa Kömür, et al.Journal of Child Neurology|August 4, 2025
Clinicoradiologic Features and Genetic Findings of Infantile Neuroaxonal DystrophyEsra Sarigecili, Habibe Koc Ucar, Sevcan Tug Bozdogan, et al.The Breast Journal|June 23, 2019
BRCA mutation characteristics in a series of index cases of breast cancer selected independent of family historyAtil Bisgin, Ibrahim Boga, Orcun Yalav, et al.Annals of Indian Academy of Neurology|February 24, 2021
Identification of a Novel Mutation in <i>GRIN2A</i> Gene with Global Developmental Delay and Refractory EpilepsyEsra Sarigecili, Meltem Cobanogullari Direk, Mustafa Komur, et al.Journal of Pediatric Genetics|November 6, 2024
<i>CYP1B1</i> and <i>MYOC</i> Gene Analysis of Patients with Primary Congenital Glaucoma in the Cukurova Region of TürkiyeAhsen Cavusoglu Akbas, Elif Erdem, Sevcan Tug Bozdogan, et al.Clinical Psychopharmacology and Neuroscience : the Official Scientific Journal of the Korean College of Neuropsychopharmacology|November 24, 2018
No Association between Polymorphisms of Vitamin D and Oxytocin Receptor Genes and Autistic Spectrum Disorder in a Sample of Turkish ChildrenSevcan Tug Bozdogan, Meryem Ozlem Kutuk, Evren Tufan, et al.Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|April 1, 2015
Alpha-thalassemia mutations in adana province, southern Turkey: genotype-phenotype correlationSevcan Tug Bozdogan, Ozge Ozalp Yuregir, Nurhilal Buyukkurt, et al.Hemoglobin|March 6, 2012
Nonsense β-thalassemia mutation at codon 37 (TGG>TGA), detected for the first time in three Turkish casesSevcan Tug Bozdogan, Cagatay Unsal, Hakan Erkman, et al.Archives of Medical Science : AMS|October 12, 2012
β-Globin chain abnormalities with coexisting α-thalassemia mutationsBirol Guvenc, Abdullah Canataroglu, Cagatay Unsal, et al.Pageof 2