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Child with RET proto-oncogene codon 634 mutation.
İnce D, Demirağ B, Ataseven E, Oymak Y, Tuhan H, Karakuş OZ, Hazan F, Abacı A, Özer E, Mutafoglu K, Olgun N. İnce D, et al. Among authors: hazan f. Turk J Pediatr. 2017;59(5):590-593. doi: 10.24953/turkjped.2017.05.014. Turk J Pediatr. 2017. PMID: 29745123 Free article.
Ince D, Demirag B, Ataseven E, Oymak Y, Tuhan H, Karakus OZ, Hazan F, Abaci A, Ozer E, Mutafoglu K, Olgun N. Child with RET proto-oncogene codon 634 mutation. ...
Ince D, Demirag B, Ataseven E, Oymak Y, Tuhan H, Karakus OZ, Hazan F, Abaci A, Ozer E, Mutafoglu K, Olgun N. Child with RET pr …
Chronic Neutropenia in Childhood: Experience From a Single Center.
Karapinar TH, Oymak Y, Ay Y, Köker SA, Töret E, Hazan F, Vergin C. Karapinar TH, et al. Among authors: hazan f. J Pediatr Hematol Oncol. 2016 Jan;38(1):e35-8. doi: 10.1097/MPH.0000000000000449. J Pediatr Hematol Oncol. 2016. PMID: 26479986
Childhood onset limb-girdle muscular dystrophies in the Aegean part of Turkey.
Yiş U, Diniz G, Hazan F, Daimagüler HS, Baysal BT, Baydan F, Akinci G, Ünalp A, Aktan G, Bayram E, Hiz S, Paketçi C, Okur D, Özer E, Danyeli AE, Polat M, Uyanik G, Çirak S. Yiş U, et al. Among authors: hazan f. Acta Myol. 2018 Sep 1;37(3):210-220. eCollection 2018 Sep. Acta Myol. 2018. PMID: 30838351 Free PMC article.
The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome.
Gürsoy S, Kutbay YB, Özdemir TR, Hazan F. Gürsoy S, et al. Among authors: hazan f. Turk J Pediatr. 2019;61(4):589-593. doi: 10.24953/turkjped.2019.04.017. Turk J Pediatr. 2019. PMID: 31990478 Free article.
Gursoy S, Kutbay YB, Ozdemir TR, Hazan F. The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome. ...
Gursoy S, Kutbay YB, Ozdemir TR, Hazan F. The clinical and molecular features of three Turkish patients with a rare genetic di …
A Neonatal Case of Infantile Malignant Osteopetrosis Presenting with Thrombocytopenia and Hypotonicity: A Novel Mutation in Chloride Voltage-Gated Channel 7 Gene.
Odaman Al I, Oymak Y, Hazan F, Gursoy S, Ozturk T, Bag O, Gozmen S, Karakaya N, Karapinar TH. Odaman Al I, et al. Among authors: hazan f. Sisli Etfal Hastan Tip Bul. 2022 Mar 28;56(1):161-165. doi: 10.14744/SEMB.2021.88964. eCollection 2022. Sisli Etfal Hastan Tip Bul. 2022. PMID: 35515972 Free PMC article.
58 results