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Page 1
A novel missense mutation of the GRK1 gene in Oguchi disease.
Teke MY, Citirik M, Kabacam S, Demircan S, Alikasifoglu M. Teke MY, et al. Among authors: kabacam s. Mol Med Rep. 2016 Oct;14(4):3129-33. doi: 10.3892/mmr.2016.5620. Epub 2016 Aug 9. Mol Med Rep. 2016. PMID: 27511724 Free PMC article.
Genetic IGF1R defects: new cases expand the spectrum of clinical features.
Gonc EN, Ozon ZA, Oguz S, Kabacam S, Taskiran EZ, Kiper POS, Utine GE, Alikasifoglu A, Kandemir N, Boduroglu OK, Alikasifoglu M. Gonc EN, et al. Among authors: kabacam s. J Endocrinol Invest. 2020 Dec;43(12):1739-1748. doi: 10.1007/s40618-020-01264-y. Epub 2020 Apr 30. J Endocrinol Invest. 2020. PMID: 32356191
Clinical and molecular evaluation of 16 patients with Rett syndrome.
Zengin-Akkuş P, Taşkıran EZ, Kabaçam S, Şimşek-Kiper PÖ, Haliloğlu G, Boduroğlu K, Utine GE. Zengin-Akkuş P, et al. Among authors: kabacam s. Turk J Pediatr. 2018;60(1):1-9. doi: 10.24953/turkjped.2018.01.001. Turk J Pediatr. 2018. PMID: 30102473 Free article.