Blau syndrome with a rare mutation in exon 9 of NOD2 gene
Velickovic, Jelena, Silan, Fatma, Bir, Firdevs Dincsoy, Silan, Coskun, Albuz, Burcu, Ozdemir, Ozturk
Published in Autoimmunity (Chur, Switzerland) (17.11.2019)
Published in Autoimmunity (Chur, Switzerland) (17.11.2019)
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Journal Article
New results for monogenic diabetes with analysis of causative genes using next-generation sequencing: a tertiary centre experience from Turkey
Karakilic, Ersen, Saygili, Emre Sedar, Silan, Fatma, Onduc, Gonca Gul, Agcaoglu, Ugurcan
Published in International journal of diabetes in developing countries (01.10.2022)
Published in International journal of diabetes in developing countries (01.10.2022)
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Journal Article
Warfarin Resistance: A Case Report
Gönlügür, Uğur, Gönlügür, Tanseli, Özdemir, Öztürk, Sılan, Fatma
Published in Eurasian journal of emergency medicine (01.03.2019)
Published in Eurasian journal of emergency medicine (01.03.2019)
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Journal Article
Recurrent pregnancy loss and its relation to combined parental thrombophilic gene mutations
Ozdemir, Oztürk, Yenicesu, Gonca Imir, Silan, Fatma, Köksal, Binnur, Atik, Sinem, Ozen, Filiz, Göl, Mert, Cetin, Ali
Published in Genetic testing and molecular biomarkers (01.04.2012)
Published in Genetic testing and molecular biomarkers (01.04.2012)
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Journal Article
Germ-line MTHFR C677T, FV H1299R and PAI-1 5G/4G variations in breast carcinoma
Ozen, Filiz, Erdis, Eda, Sik, Ebru, Silan, Fatma, Uludag, Ahmet, Ozdemir, Ozturk
Published in Asian Pacific journal of cancer prevention : APJCP (01.01.2013)
Published in Asian Pacific journal of cancer prevention : APJCP (01.01.2013)
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Journal Article
The clinical, cytogenetics and molecular characterization of inverted duplication/deletion of chromosome 8p in a boy with mental and motor retardation: Genotype-phenotype correlation in a case report
Silan, Fatma, Bourouba, Romyla, Karakaya, Taner, Yildiz, Onur, Paksoy, Baris, Urfali, Mine, Ozdemir, Ozturk
Published in The Egyptian journal of medical human genetics (01.10.2018)
Published in The Egyptian journal of medical human genetics (01.10.2018)
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Journal Article
Is there any increased risk of hypertension, diabetes and cardiac diseases in psoriatic patients with TNF-α G238A and G308A polymorphism?
Işik, Selda, Hız, Meliha Merve, Kılıç, Sevilay, Öğretmen, Zerrin, Silan, Fatma
Published in Postȩpy dermatologii i alergologii (01.12.2016)
Published in Postȩpy dermatologii i alergologii (01.12.2016)
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Journal Article
Association Between Inherited Thrombophilia and Impaired Right Ventricular Function in Deep Vein Thrombosis Without Symptomatic Pulmonary Embolism
Asgun, Halil Fatih, Kirilmaz, Bahadir, Saygi, Serkan, Ozturk, Okan, Silan, Fatma, Karatag, Ozan, Kosar, Sule, Ozdemir, Ozturk
Published in Clinical and applied thrombosis/hemostasis (01.04.2014)
Published in Clinical and applied thrombosis/hemostasis (01.04.2014)
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Journal Article
Possible Roles of the Xenobiotic Transporter P-glycoproteins Encoded by the MDR1 3435 C＞T Gene Polymorphism in Differentiated Thyroid Cancers
Ozdemir, Semra, Uludag, Ahmet, Silan, Fatma, Atik, Sinem Yalcintepe, Turgut, Bulent, Ozdemir, Ozturk
Published in Asian Pacific journal of cancer prevention : APJCP (2013)
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Published in Asian Pacific journal of cancer prevention : APJCP (2013)
Journal Article
A case report of a patient with neurodevelopmental disorder with impaired speech and hyperkinetic movements: A biallelic variant in the ZNF142 gene
Kaya, Derya, Ceylan Köse, Canan, Akcan, Mehmet Berkay, Silan, Fatma
Published in American journal of medical genetics. Part A (01.09.2024)
Published in American journal of medical genetics. Part A (01.09.2024)
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Journal Article
Anemia and thrombocytopenia due to a novel BRPF1 variant in a family from Çanakkale with intellectual disability and dysmorphic facies: Case report and review of the literature
Kose, Canan Ceylan, Kaya, Derya, Akcan, Mehmet Berkay, Silan, Fatma
Published in American journal of medical genetics. Part A (01.08.2023)
Published in American journal of medical genetics. Part A (01.08.2023)
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Journal Article