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Autori: Ozdemir Ozturk

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Naslov 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 (Article)
Autori Dincsoy Bir Firdevs Silan Fatma Velickovic Jelena  Berkay Akcan Mehmet Ozdemir Ozturk 
Info MOLECULAR SYNDROMOLOGY, (2022), vol. 13 br. 3, str. 254-260
Projekat Scientific Research Foundation Unit (BAP) of Canakkale Onsekiz Mart University, Canakkale-Turkey [BAP-TAY2015/445]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Blau syndrome with a rare mutation in exon 9 of NOD2 gene (Article)
Autori Velickovic Jelena  Silan Fatma Bir Firdevs Dincsoy Silan Coskun Albuz Burcu Ozdemir Ozturk 
Info AUTOIMMUNITY, (2019), vol. 52 br. 7-8, str. 256-263
Projekat Scientific Research Foundation Unit (BAP) of Canakkale Onsekiz Mart University, Canakkale-Turkey [BAP - 2014/227]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Rare disease or rare diagnosed diseases: Blau syndrome with a rare mutation in exon 9 of NOD2 gene from Canakkale (Meeting Abstract)
Autori Silan Fatma Djurovic Jelena  Bir Firdevs Dincsoy Silan Coskun Ozdemir Ozturk 
Info JOURNAL OF BIOTECHNOLOGY, (2018), vol. 280 br. , Suppl. S, str. S65-S65
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Association between FokI, ApaI and TaqI RFLP polymorphisms in VDR gene and Hashimoto's thyroiditis: preliminary data from female patients in Serbia (Article)
Autori Djurovic Jelena  Stojkovic Oliver V Ozdemir Ozturk Silan Fatma Akurut C Todorovic Jelena Savic Kristina Stamenkovic Gorana G  
Info INTERNATIONAL JOURNAL OF IMMUNOGENETICS, (2015), vol. 42 br. 3, str. 190-194
Projekat Serbian Ministry of Education, Science and Technology [OI 175093]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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