@ARTICLE{
author={Dincsoy Bir Firdevs,Silan Fatma,Velickovic Jelena,Berkay Akcan Mehmet,Ozdemir Ozturk},
year={2022},
title={A New Case of Rare Microdeletion 10q22.3q23 along with Mosaic Klinefelter Syndrome Associated with Facial Dysmorphic Finding, Atrial Ventricular Septal Defect, and Motor Retardation},
journal={MOLECULAR SYNDROMOLOGY},
volume={13},
number={3},
pages={254-260},
document_type={Article},
} 

@ARTICLE{
author={Velickovic Jelena,Silan Fatma,Bir Firdevs Dincsoy,Silan Coskun,Albuz Burcu,Ozdemir Ozturk},
year={2019},
title={Blau syndrome with a rare mutation in exon 9 of NOD2 gene},
journal={AUTOIMMUNITY},
volume={52},
number={7-8},
pages={256-263},
document_type={Article},
} 

@ARTICLE{
author={Silan Fatma,Djurovic Jelena,Bir Firdevs Dincsoy,Silan Coskun,Ozdemir Ozturk},
year={2018},
title={Rare disease or rare diagnosed diseases: Blau syndrome with a rare mutation in exon 9 of NOD2 gene from Canakkale},
journal={JOURNAL OF BIOTECHNOLOGY},
volume={280},
number={},
pages={S65-S65},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Djurovic Jelena,Stojkovic Oliver V,Ozdemir Ozturk,Silan Fatma,Akurut C,Todorovic Jelena,Savic Kristina,Stamenkovic Gorana G},
year={2015},
title={Association between FokI, ApaI and TaqI RFLP polymorphisms in VDR gene and Hashimoto's thyroiditis: preliminary data from female patients in Serbia},
journal={INTERNATIONAL JOURNAL OF IMMUNOGENETICS},
volume={42},
number={3},
pages={190-194},
document_type={Article},
}