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2023 7
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Page 1
Clinical Features of Aberrations Chromosome 22q: A Pilot Study.
Atli EI, Atli E, Yalcintepe S, Demir S, Mail C, Eker D, Ozen Y, Gurkan H. Atli EI, et al. Among authors: gurkan h. Glob Med Genet. 2021 Nov 9;9(1):42-50. doi: 10.1055/s-0041-1739496. eCollection 2022 Mar. Glob Med Genet. 2021. PMID: 35169783 Free PMC article.
Prenatal diagnosis of 20p13 microdeletion syndrome.
Yener C, Sayın C, İnan C, Gürkan H, Atlı Eİ, Atlı E, Altan E, Ateş S, Varol F. Yener C, et al. Among authors: gurkan h. Taiwan J Obstet Gynecol. 2021 Mar;60(2):350-354. doi: 10.1016/j.tjog.2021.01.015. Taiwan J Obstet Gynecol. 2021. PMID: 33678341 Free 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 S, Tozkir H, Y… See abstract for full author list ➔ Dundar M, et al. Among authors: gurkan h. 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 Genetics Study in the Foreskin of Boys with Hypospadias.
Inanc I, Avlan D, Eker D, Gurkan H. Inanc I, et al. Among authors: gurkan h. Mol Syndromol. 2023 Jun;14(3):185-190. doi: 10.1159/000527405. Epub 2023 Jan 16. Mol Syndromol. 2023. PMID: 37323199 Free PMC article.
Clinical Implications of Chromosome 16 Copy Number Variation.
Atli EI, Yalcintepe S, Atli E, Demir S, Mail C, Gurkan H. Atli EI, et al. Among authors: gurkan h. Mol Syndromol. 2022 May;13(3):184-192. doi: 10.1159/000517762. Epub 2021 Dec 15. Mol Syndromol. 2022. PMID: 35707588 Free PMC article.
Novel EYA1 variants causing Branchio-oto-renal syndrome.
Klingbeil KD, Greenland CM, Arslan S, Llamos Paneque A, Gurkan H, Demir Ulusal S, Maroofian R, Carrera-Gonzalez A, Montufar-Armendariz S, Paredes R, Elcioglu N, Menendez I, Behnam M, Foster J 2nd, Guo S, Escarfuller S, Cengiz FB, Duman D, Bademci G, Tekin M. Klingbeil KD, et al. Among authors: gurkan h. Int J Pediatr Otorhinolaryngol. 2017 Jul;98:59-63. doi: 10.1016/j.ijporl.2017.04.037. Epub 2017 Apr 26. Int J Pediatr Otorhinolaryngol. 2017. PMID: 28583505 Free PMC article.
A Case of Diabetes Mellitus Type MODY5 as a feature of 17q12 Deletion Syndrome.
Yaşar Köstek H, Özgüç Çömlek F, Gürkan H, Özkayın EN, Tütüncüler Kökenli F. Yaşar Köstek H, et al. Among authors: gurkan h. J Clin Res Pediatr Endocrinol. 2022 Dec 13. doi: 10.4274/jcrpe.galenos.2022.2022-3-2. Online ahead of print. J Clin Res Pediatr Endocrinol. 2022. PMID: 36511482 Free article.
83 results