Autori: Silan Fatma
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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