Epilepsi ve anlıksal yetiyitimi olan hastalarda moleküler karyotiplemenin klinik yararı

by Atıl BİŞGİN, Sevcan TUĞ BOZDOĞAN
Published 2018-12-01

Hereditary spastic paraplegia type 35 with a novel mutation in fatty acid 2-hydroxylase gene and literature review of the clinical features

by Faruk Incecik, Seyda Besen, Sevcan Tug Bozdogan
Published 2018-01-01

A Case with Mental Retardation, Gynecomastia and Dysmorphic Features

by Ozge Ozalp Yuregir, Huseyin Aslan, Sevcan Tug Bozdogan, Muhammed Hamza Muslumanoglu
Published 2012-03-01

A Case with Mental Retardation, Gynecomastia and Dysmorphic Features

by Ozge Ozalp Yuregir, Huseyin Aslan, Sevcan Tug Bozdogan, Muhammed Hamza Muslumanoglu
Published 2012-02-01

Familial hypertrophic cardiomyopathy: A case with a new mutation in the MYBPC3 gene

by Olgu Hallioglu Kilinc, Dilek Giray, Atil Bisgin, Sevcan Tug Bozdogan, Derya Karpuz
Published 2017-07-01

Identification of a novel mutation in GRIN2A gene with global developmental delay and refractory epilepsy

by Esra Sarigecili, Meltem Cobanogullari Direk, Mustafa Komur, Sevcan Tug Bozdogan, Cetin Okuyaz
Published 2020-01-01

Dysarthria, ataxia, and dystonia associated with COX20 (FAM36A) gene mutation: A case report of a Turkish child

by Duygu G Ozcanyuz, Faruk Incecik, Ozlem M Herguner, Neslihan O Mungan, Sevcan T Bozdogan
Published 2020-01-01

Vandetanib in a Child Affected by Neurofibromatosis Type 1 and Medullary Thyroid Carcinoma with Both NF1 and Homozygous RET Proto-oncogen Germ-line Mutations

by Begümhan Demir Gündoğan, Fatih Sağcan, Sevcan Tuğ Bozdoğan, Yüksel Balcı, Ferah Tuncel Daloğlu, Elvan Cağlar Çıtak
Published 2021-09-01

Current Status of Genetic Diagnosis Laboratories and Frequency of Genetic Variants Associated with Cystic Fibrosis through a Newborn-Screening Program in Turkey

by Sevcan Tug Bozdogan, Cem Mujde, Ibrahim Boga, Ozge Sonmezler, Abdullah Hanta, Cagla Rencuzogullari, Dilek Ozcan, Derya Ufuk Altintas, Atil Bisgin
Published 2021-01-01