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A newborn with monosomy X in association with corpus callosum agenesis.
Onur Cura D, Iscan B, Gursoy S, Guleryuz H, Cankaya T, Ozturk T, Giray Bozkaya O. Onur Cura D, et al. Among authors: cankaya t. Pediatr Neonatol. 2017 Oct;58(5):455-457. doi: 10.1016/j.pedneo.2016.05.006. Epub 2016 Nov 28. Pediatr Neonatol. 2017. PMID: 28117231 Free article. No abstract available.
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: cankaya t. 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: cankaya t. 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.
47 results