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First-Line Molecular Genetic Evaluation of Autosomal Recessive Non-Syndromic Hearing Loss.
Özyılmaz B, Mercan GC, Kırbıyık Ö, Özdemir TR, Özkara S, Kaya ÖÖ, Kutbay YB, Erdoğan KM, Güvenç MS, Koç A. Özyılmaz B, et al. Among authors: guvenc ms. Turk Arch Otorhinolaryngol. 2019 Sep;57(3):140-148. doi: 10.5152/tao.2019.4320. Epub 2019 Sep 1. Turk Arch Otorhinolaryngol. 2019. PMID: 31620696 Free PMC article.
Evaluation of chromosomal abnormalities and Y-chromosome microdeletions in 1696 Turkish cases with primary male infertility: A single-center study.
Özdemir TR, Özyılmaz B, Çakmak Ö, Kaya ÖÖ, Köse C, Kırbıyık Ö, Keskin MZ, Koç A, Zeyrek T, Kutbay YB, Erdoğan KM, Güvenç MS. Özdemir TR, et al. Among authors: guvenc ms. Turk J Urol. 2019 Nov 29;46(2):95-100. doi: 10.5152/tud.2019.19156. Print 2020 Mar. Turk J Urol. 2019. PMID: 32125967 Free PMC article.
Experiences in the molecular genetic and histopathological evaluation of calpainopathies.
Ozyilmaz B, Kirbiyik O, Ozdemir TR, Ozer OK, Kutbay YB, Erdogan KM, Guvenc MS, Arıkan Ş, Turk TS, Kale MY, Uludag IF, Baydan F, Sertpoyraz F, Gencpinar P, Diniz G. Ozyilmaz B, et al. Among authors: guvenc ms. Neurogenetics. 2022 Apr;23(2):103-114. doi: 10.1007/s10048-022-00687-4. Epub 2022 Feb 14. Neurogenetics. 2022. PMID: 35157181
14 results