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Genetic Evaluation of Common Neurocutaneous Syndromes.
Gürsoy S, Erçal D. Gürsoy S, et al. Among authors: ercal d. Pediatr Neurol. 2018 Dec;89:3-10. doi: 10.1016/j.pediatrneurol.2018.08.006. Epub 2018 Aug 10. Pediatr Neurol. 2018. PMID: 30424961 Review.
Identification of PCDH19 Gene Mutations/Deletions in Patients with Early Onset Epilepsy.
Gursoy S, Ataman E, Baysal BT, Özyılmaz B, Gençpınar P, Hız AS, Yiş U, Ünalp A, Dündar NO, Ülgenalp A, Erçal D. Gursoy S, et al. Among authors: ercal d. Ann Indian Acad Neurol. 2020 Mar-Apr;23(2):206-210. doi: 10.4103/aian.AIAN_465_19. Epub 2020 Feb 25. Ann Indian Acad Neurol. 2020. PMID: 32189863 Free PMC article.
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: ercal d. 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: ercal d. 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.
49 results