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Vanishing white matter disease with different faces.
Güngör G, Güngör O, Çakmaklı S, Maraş Genç H, İnce H, Yeşil G, Dilber C, Aydın K. Güngör G, et al. Among authors: cakmakli s. Childs Nerv Syst. 2020 Feb;36(2):353-361. doi: 10.1007/s00381-019-04334-6. Epub 2019 Aug 5. Childs Nerv Syst. 2020. PMID: 31385086
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. Cytogenet Genome Res. 2017;153(4):175-180. doi: 10.1159/000486775. Epub 2018 Mar 9. Cytogenet Genome Res. 2017. PMID: 29518772 Review.
12 results