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Autori: Silan Fatma

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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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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