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Year Number of Results
2007 1
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2014 1
2015 4
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2018 6
2019 12
2020 3
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2024 1

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Page 1
Clinical and genetic spectrum from a prototype of ciliopathy: Joubert syndrome.
Aksu Uzunhan T, Ertürk B, Aydın K, Ayaz A, Altunoğlu U, Yarar MH, Gezdirici A, İçağasıoğlu DF, Gökpınar İli E, Uyanık B, Eser M, Kutbay YB, Topçu Y, Kılıç B, Bektaş G, Arduç Akçay A, Ekici B, Chousein A, Avcı Ş, Yüksel A, Kayserili H. Aksu Uzunhan T, et al. Clin Neurol Neurosurg. 2023 Jan;224:107560. doi: 10.1016/j.clineuro.2022.107560. Epub 2022 Dec 13. Clin Neurol Neurosurg. 2023. PMID: 36580738
Nevus-like lesions on the lip and the foot.
Kutbay NO, Yurekli BS, Sever A, Ceylan C. Kutbay NO, et al. Eur J Intern Med. 2018 Jul;53:e6-e7. doi: 10.1016/j.ejim.2017.12.017. Epub 2018 Jan 12. Eur J Intern Med. 2018. PMID: 29336867 No abstract available.
A case of idiopathic granulomatous hypophysitis.
Kutbay NO, Berker M, Soylemezoglu F, Ozisik H, Yurekli BS. Kutbay NO, et al. Hormones (Athens). 2017 Jul;16(3):331-332. doi: 10.14310/horm.2002.1752. Hormones (Athens). 2017. PMID: 29278522 Free article. No abstract available.
Fetal HLA-G alleles and their effect on miscarriage.
Koc A, Kirbiyik O, Kutbay YB, Ozyilmaz B, Ozdemir TR, Kaya OO, Kubat G, Koc ZP. Koc A, et al. Adv Clin Exp Med. 2018 Sep;27(9):1233-1237. doi: 10.17219/acem/69692. Adv Clin Exp Med. 2018. PMID: 29809322 Free article.
The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome.
Gürsoy S, Kutbay YB, Özdemir TR, Hazan F. Gürsoy S, et al. Turk J Pediatr. 2019;61(4):589-593. doi: 10.24953/turkjped.2019.04.017. Turk J Pediatr. 2019. PMID: 31990478 Free article.
Gursoy S, Kutbay YB, Ozdemir TR, Hazan F. The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome. ...
Gursoy S, Kutbay YB, Ozdemir TR, Hazan F. The clinical and molecular features of three Turkish patients with a rare genetic disorder: …
44 results