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Genetic background of supernumerary teeth.
Subasioglu A, Savas S, Kucukyilmaz E, Kesim S, Yagci A, Dundar M. Subasioglu A, et al. Among authors: dundar m. Eur J Dent. 2015 Jan-Mar;9(1):153-158. doi: 10.4103/1305-7456.149670. Eur J Dent. 2015. PMID: 25713500 Free PMC article. Review.
A Glutamine Repeat Variant of the RUNX2 Gene Causes Cleidocranial Dysplasia.
Mastushita M, Kitoh H, Subasioglu A, Kurt Colak F, Dundar M, Mishima K, Nishida Y, Ishiguro N. Mastushita M, et al. Among authors: dundar m. Mol Syndromol. 2015 Feb;6(1):50-3. doi: 10.1159/000370337. Epub 2015 Jan 29. Mol Syndromol. 2015. PMID: 25852448 Free PMC article.
Research of genetic bases of hereditary non-syndromic hearing loss.
Subaşıoğlu A, Duman D, Sırmacı A, Bademci G, Carkıt F, Somdaş MA, Erkan M, Tekin M, Dündar M. Subaşıoğlu A, et al. Among authors: dundar m. Turk Pediatri Ars. 2017 Sep 1;52(3):122-132. doi: 10.5152/TurkPediatriArs.2017.4254. eCollection 2017 Sep. Turk Pediatri Ars. 2017. PMID: 29062245 Free PMC article.
Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium.
Dundar M, Fahrioglu U, Yildiz SH, Bakir-Gungor B, Temel SG, Akin H, Artan S, Cora T, Sahin FI, Dursun A, Sezer O, Gurkan H, Erdogan M, Gunduz CNS, Bisgin A, Ozdemir O, Ulgenalp A, Percin EF, Yildirim ME, Tekes S, Bagis H, Yuce H, Duman N, Bozkurt G, Yararbas K, Yildirim MS, Arman A, Mihci E, Eraslan S, Altintas ZM, Aymelek HS, Ruhi HI, Tatar A, Ergoren MC, Cetin GO, Altunoglu U, Caglayan AO, Yuksel B, Ozkul Y, Saatci C, Kenanoglu S, Karasu N, Dundar B, Ozcelik F, Demir M, Siniksaran BS, Kulak H, Kiranatlioglu K, Baysal K, Kazimli U, Akalin H, Dundar A, Boz M, Bayram A, Subasioglu A, Colak FK, Karaduman N, Gunes MC, Kandemir N, Aynekin B, Emekli R, Sahin IO, Ozdemir SY, Onal MG, Senel AS, Poyrazoglu MH, Kisaarslan ANP, Gursoy S, Baskol M, Calis M, Demir H, Zararsiz GE, Erdogan MO, Elmas M, Solak M, Ulu MS, Thahir A, Aydin Z, Atasever U, Sag SO, Aliyeva L, Alemdar A, Dogan B, Erguzeloglu CO, Kaya N, Ozkinay F, Cogulu O, Durmaz A, Onay H, Karaca E, Durmaz B, Aykut A, Cilingir O, Aras BD, Gokalp EE, Arslan S, Temena A, Haziyeva K, Kocagil S, Bas H, Susam E, Keklikci AR, Sarac E, Kocak N, Nergiz S, Terzi YK, Dincer SA, Baskin ES, Genc GC, Bahadir O, Sanri A, Yigit … See abstract for full author list ➔ Dundar M, et al. Among authors: dundar b, dundar a. Funct Integr Genomics. 2022 Jun;22(3):291-315. doi: 10.1007/s10142-021-00819-3. Epub 2022 Jan 31. Funct Integr Genomics. 2022. PMID: 35098403
Frank-ter Haar syndrome with unusual clinical features.
Dundar M, Saatci C, Tasdemir S, Akcakus M, Caglayan AO, Ozkul Y. Dundar M, et al. Eur J Med Genet. 2009 Jul-Aug;52(4):247-9. doi: 10.1016/j.ejmg.2009.03.005. Epub 2009 Mar 19. Eur J Med Genet. 2009. PMID: 19303467
Evaluation of chromosomal abnormalities in the postnatal cohort: A single-center study on 14,242 patients.
Akalin H, Sahin IO, Paskal SA, Tan B, Yalcinkaya E, Demir M, Yakubi M, Caliskan BO, Ekinci OG, Ercan M, Kucuk TY, Gokgoz G, Kiraz A, Per H, Ozgun MT, Baydilli N, Ozkul Y, Dundar M. Akalin H, et al. Among authors: dundar m. J Clin Lab Anal. 2024 Jan;38(1-2):e24997. doi: 10.1002/jcla.24997. Epub 2023 Dec 19. J Clin Lab Anal. 2024. PMID: 38115218 Free PMC article.
286 results