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Öztürk Özdemir

Ataturk University

19H指数
273论文数
1.3K被引数
收录论文 27
发表时间
Blau syndrome with a rare mutation in exon 9 of NOD2 gene
err2019-09-26
err6
PREAI
errVelickovic, Jelena; Silan, Fatma; Bir, Firdevs Dincsoy; Silan, Coskun; Albuz, Burcu; Ozdemir, Ozturk
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The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance
err2019-07-01
err78
errOAAI
errPehlivan, Davut; Bayram, Yavuz; Gunes, Nilay; Akdemir, Zeynep Coban; Shukla, Anju; Bierhals, Tatjana; Tabakci, Burcu; Sahin, Yavuz; Gezdirici, Alper; Fatih, Jawid M.; Gulec, Elif Yilmaz; Yesil, Gozde; Punetha, Jaya; Ocak, Zeynep; Grochowski, Christopher M.; Karaca, Ender; Albayrak, Hatice Mutlu; Radhakrishnan, Periyasamy; Erdem, Haktan Bagis; Sahin, Ibrahim; Yildirim, Timur; Bayhan, Ilhan A.; Bursali, Aysegul; Elmas, Muhsin; Yuksel, Zafer; Ozdemir, Ozturk; Silan, Fatma; Yildiz, Onur; Yesilbas, Osman; Isikay, Sedat; Balta, Burhan; Gu, Shen; Jhangiani, Shalini N.; Doddapaneni, Harsha; Hu, Jianhong; Muzny, Donna M.; Boerwinkle, Eric; Gibbs, Richard A.; Tsiakas, Konstantinos; Hempel, Maja; Girisha, Katta Mohan; Gul, Davut; Posey, Jennifer E.; Elcioglu, Nursel H.; Tuysuz, Beyhan; Lupski, James R.
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Frameshift mutation in N-acetyl-glutamate synthase (NAGS) gene in a consanguineous family: three deceased cases before diagnosis
err2018-08-01
err0
PREAI
errSilan, Fatma; Karakaya, Taner; Bir, Firdevs Dincsoy; Paksoy, Baris; Ozdemir, Ozturk
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A case with 10q22.3q23.2 microdeletion syndrome and mosaic Klinefelter syndrome
err2018-08-01
err0
PREAI
errBir, Firdevs Dincsoy; Ozdemir, Ozturk; Karakaya, Taner; Yildiz, Onur; Silan, Fatma
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Rare disease or rare diagnosed diseases: Blau syndrome with a rare mutation in exon 9 of NOD2 gene from Canakkale
err2018-08-01
err0
PREAI
errSilan, Fatma; Djurovic, Jelena; Bir, Firdevs Dincsoy; Silan, Coskun; Ozdemir, Ozturk
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A mental and motor retarded case with derivative chromosome 8p rearrangements: Genotype-phenotype correlation in a case report
err2017-08-01
err0
PREAI
errSilan, Fatma; Karakaya, Taner; Yildiz, Onur; Paksoy, Baris; Urfali, Mine; Ozdemir, Ozturk
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Possible association between germline methylenetetrahydrofolate reductase gene polymorphisms and psoriasis risk in a Turkish population
err2016-12-27
err8
PREAI
errKilic, S.; Ozdemir, O.; Silan, F.; Isik, S.; Yildiz, O.; Karaagacli, D.; Silan, C.; Ogretmen, Z.
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Assessment of BMP-6 polymorphism and relationship with disease activity in Ankylosing Spondylitis patients
err2016-08-01
err0
PREAI
errOztopuz, R. Ozlem; Silan, Fatma; Akbal, Ayla; Coskun, Ozlem; Ozdemir, Ozturk
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Alterations in the telomere length distribution of cell-free DNA in human cancer
err2016-08-01
err0
PREAI
errUrfali, Mine; Silan, Fatma; Tan, Yusuf Ziya; Celiker, Fatmanur; Guler, Zeliha; Ozdemir, Ozturk
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The thrombophilic gene polymorphisms and recurrent pregnancy loss dilemma: From Minsk/Belarus and Canakkale - Sivas/Turkish populations
err2016-08-01
err0
PREAI
errSilan, Fatma; Mosse, Irma; Gonchar, Alexander; Sedlyar, Nikita; Kilchevsky, Alexander V.; Kuru, Banu; Ozdemir, Ozturk; Ozdemir, Ozturk
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The microdeletion/microduplication profiles in spontaneously aborted fetal materials: Double blind results of QF-PCR and MLPA techniques
err2015-08-01
err0
PREAI
errSilan, Fatma; Ari, Elif; Uludag, Ahmet; Yildiz, Onur; Isin, Betul; Paksoy, Baris; Urfali, Mine; Ozdemir, Ozturk
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The RFLP profiles at BRAF V600E mutations in thyroid FNAB nodules
err2015-08-01
err0
PREAI
errOzdemir, Semra; Asik, Mehmet; Silan, Fatma; Ozdemir, Ozturk; Tan, Yusuf Ziya; Ari, Elif; Eroglu, Mustafa; Ukinc, Kubilay
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