Fahrettin Duymus

A Case Report of Neurofibromatosis Type 1 Diagnosed with a Noval Mutation Detection in NF1 Gene

N. Koçak, T. Cora, Nafiz Yaşa, 2019, Selcuk Tip Dergisi.

Relationship of endoplasmic reticulum stress with the etiopathogenesis of chronic tonsillitis and tonsillar hypertrophy in pediatric patients: a prospective, parallel-group study

O. Erdur, M. Bozkurt, O. Onal, 2021, Molecular Biology Reports.

In silico analysis of similar protein sequences between Sars-Cov-2 and BCG vaccine

N. Koçak, D. Esin, E. Ozdemir, 2021, Molecular Genetics and Metabolism.

A novel double hemizygous BTK mutation in a boy presenting with Pseudomonas skin abscesses

H. Artaç, Melike Emiroğlu, Fahrettin Duymus, 2022, Clinical and experimental dermatology.

SYNGAP1 mutation in a pediatric patient with autism spectrum disorder and intellectual disability

F. Çetin, S. Türkoğlu, T. Cora, 2020, Dusunen Adam: The Journal of Psychiatry and Neurological Sciences.

THE CASE OF WİLLİAMS-BEUREN SYNDROME DİAGNOSED İN İNFANCY : THE İMPORTANCE OF EARLY DİAGNOSİS

F. Bugrul, Fahrettin Duymus, 2019, Journal of Contemporary Medicine.