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Page 1
The molecular basis and genotype-phenotype correlations of congenital adrenal hyperplasia (CAH) in Anatolian population.
Dundar A, Bayramov R, Onal MG, Akkus M, Dogan ME, Kenanoglu S, Cerrah Gunes M, Kazimli U, Ozbek MN, Ercan O, Yildirim R, Celmeli G, Parlak M, Dundar I, Hatipoglu N, Unluhizarci K, Akalin H, Ozkul Y, Saatci C, Dundar M. Dundar A, et al. Among authors: saatci c. Mol Biol Rep. 2019 Aug;46(4):3677-3690. doi: 10.1007/s11033-019-04809-4. Epub 2019 Apr 20. Mol Biol Rep. 2019. PMID: 31006099
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 S, Tozkir H, Y… See abstract for full author list ➔ Dundar M, et al. Among authors: saatci c. 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
A Turner patient with a 45,X,t(1;2) (q41;p11.2) karyotype.
Ozkul Y, Atabek ME, Dundar M, Kurtoglu S, Saatci C. Ozkul Y, et al. Among authors: saatci c. Ann Genet. 2002 Oct-Dec;45(4):181-3. doi: 10.1016/s0003-3995(02)01139-5. Ann Genet. 2002. PMID: 12668164
Frank-ter Haar syndrome with unusual clinical features.
Dundar M, Saatci C, Tasdemir S, Akcakus M, Caglayan AO, Ozkul Y. Dundar M, et al. Among authors: saatci c. 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
Holt-Oram syndrome in two generations with translocation t(9;15)(p12;q11.2).
Caglayan AO, Koklu E, Saatci C, Gunes T, Ozkul Y, Narin N, Baykan A, Dundar M, Buyukkayhan D. Caglayan AO, et al. Among authors: saatci c. Ann Saudi Med. 2008 May-Jun;28(3):209-12. doi: 10.5144/0256-4947.2008.209. Ann Saudi Med. 2008. PMID: 18500176 Free PMC article. No abstract available.
27 results