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Amplification of Cellular Oncogenes in Solid Tumors.
N Am J Med Sci. 2015 Aug;7(8):341-6. doi: 10.4103/1947-2714.163641.
N Am J Med Sci. 2015.
PMID: 26417556
Free PMC article.
Review.
Frequency of mutations in Mediterranean fever gene, with gender and genotype-phenotype correlations in a Turkish population.
Coşkun S, Kurtgöz S, Keskin E, Sönmez F, Bozkurt G.
Coşkun S, et al. Among authors: kurtgoz s.
J Genet. 2015 Dec;94(4):629-35. doi: 10.1007/s12041-015-0568-z.
J Genet. 2015.
PMID: 26690517
Free article.
Item in Clipboard
A case of Ehlers-Danlos syndrome type VIA with a novel PLOD1 gene mutation.
Tosun A, Kurtgoz S, Dursun S, Bozkurt G.
Tosun A, et al. Among authors: kurtgoz s.
Pediatr Neurol. 2014 Oct;51(4):566-9. doi: 10.1016/j.pediatrneurol.2014.06.020. Epub 2014 Jul 10.
Pediatr Neurol. 2014.
PMID: 25266621
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Epithelioid hemangioendothelioma of the nasal septum.
Hanege FM, Uzun L, Yavuz C, Ozkanli S, Kurtgoz S.
Hanege FM, et al. Among authors: kurtgoz s.
B-ENT. 2016 Aug;12(2):155-157.
B-ENT. 2016.
PMID: 29553622
Review.
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A PATIENT WITH PARTIAL CHROMOSOME 12q DUPLICATION AND 10q DELETION.
Saat H, Soysal Y, Kurtgoz S, Ergun MA, Percin EF.
Saat H, et al. Among authors: kurtgoz s.
Genet Couns. 2015;26(4):401-7.
Genet Couns. 2015.
PMID: 26852510
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Assessment of nasal airway resistances and nasal mucociliary activities of patients with unilateral chronic otitis media by acoustic rhinometry and saccharin test.
Kurtgöz S, Kökten N, Tekin M.
Kurtgöz S, et al.
Acta Otolaryngol. 2014 Sep;134(9):898-903. doi: 10.3109/00016489.2014.923115. Epub 2014 Jun 30.
Acta Otolaryngol. 2014.
PMID: 24975452
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