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A toddler with a novel LEPR mutation.
Armağan C, Yılmaz C, Koç A, Abacı A, Ülgenalp A, Böber E, Erçal D, Demir K. Armağan C, et al. Among authors: koc a. Hormones (Athens). 2019 Jun;18(2):237-240. doi: 10.1007/s42000-019-00097-6. Epub 2019 Feb 18. Hormones (Athens). 2019. PMID: 30778850
Two Cases with Ring Chromosome 13 at either End of the Phenotypic Spectrum.
Çakmaklı S, Çankaya T, Gürsoy S, Koç A, Kırbıyık Ö, Kılıçarslan ÖA, Özer E, Erçal D, Bozkaya ÖG. Çakmaklı S, et al. Among authors: koc a. Cytogenet Genome Res. 2017;153(4):175-180. doi: 10.1159/000486775. Epub 2018 Mar 9. Cytogenet Genome Res. 2017. PMID: 29518772 Review.
QF-PCR in invasive prenatal diagnosis: a single-center experience in Turkey.
Özer Kaya Ö, Koç A, Özdemir TR, Kirbiyik Ö, Özyilmaz B, Özeren M, Öztekin DC, Taner CE, Kutbay YB. Özer Kaya Ö, et al. Among authors: koc a. Turk J Med Sci. 2017 Feb 27;47(1):142-147. doi: 10.3906/sag-1511-157. Turk J Med Sci. 2017. PMID: 28263482 Free article.
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: koc a. 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.
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. Among authors: koc zp. Adv Clin Exp Med. 2018 Sep;27(9):1233-1237. doi: 10.17219/acem/69692. Adv Clin Exp Med. 2018. PMID: 29809322 Free article.
571 results