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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: gursoy s. Cytogenet Genome Res. 2017;153(4):175-180. doi: 10.1159/000486775. Epub 2018 Mar 9. Cytogenet Genome Res. 2017. PMID: 29518772 Review.
Phenotypic spectrum of CHARGE syndrome based on clinical characteristics.
Aksel Kılıçarslan Ö, Ataman E, Gürsoy S, Hazan F, Randa C, Çankaya T, Erçal D, Ülgenalp A, Giray Bozkaya Ö. Aksel Kılıçarslan Ö, et al. Among authors: gursoy s. Turk J Med Sci. 2018 Oct 31;48(5):911-915. doi: 10.3906/sag-1611-107. Turk J Med Sci. 2018. PMID: 30384553 Free article.
Investigation of the most common clinical and imaging findings and the role of tubulin genes in the etiology of malformations of cortical development.
Aksel Kiliçarslan Ö, Ataman E, Gürsoy S, Gürbüz G, Ünalp A, Gençpinar P, Olgaç Dündar N, Edizer S, Ülgenalp A, Giray Bozkaya Ö. Aksel Kiliçarslan Ö, et al. Among authors: gursoy s. Turk J Med Sci. 2020 Oct 22;50(6):1573-1579. doi: 10.3906/sag-1901-170. Turk J Med Sci. 2020. PMID: 32718119 Free PMC article.
372 results