11. Novel c.1505_1509dupCTGCC pathogenic variation in a male case with Christianson syndrome. Issue 1 (January 2021) Authors: Yalcintepe, Sinem; Gurkan, Hakan Journal: Clinical dysmorphology Issue: Volume 30:Issue 1(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
12. Novel EYA1 variants causing Branchio-oto-renal syndrome. (July 2017) Authors: Klingbeil, Kyle D.; Greenland, Christopher M.; Arslan, Selcuk; Llamos Paneque, Arianne; Gurkan, Hakan; Demir Ulusal, Selma; Maroofian, Reza; Carrera-Gonzalez, Andrea; Montufar-Armendariz, Stefany; Paredes, Rosario; Elcioglu, Nursel; Menendez, Ibis; Behnam, Mahdiyeh; Foster, Joseph; Guo, Shengru; ... Journal: International journal of pediatric otorhinolaryngology Issue: Volume 98(2017:Jul.) Page Start: 59 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
13. Placental and serum levels of human Klotho in severe preeclampsia: A potential sensitive biomarker. (15th September 2019) Authors: Uzun Cilingir, Isil; Varol, Fusun; Gurkan, Hakan; Sutcu, Havva; Atli, Engin; Eker, Damla; Inan, Cihan; Erzincan, Selen; Sayin, Cenk Journal: Placenta Issue: Volume 85(2019) Page Start: 49 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
14. Prenatal diagnosis of chromosomal polymorphisms: most commonly observed polymorphism on Chromosome 9 have associations with low PAPP-A values*. (19th May 2019) Authors: Inan, Cihan; Sayin, N. Cenk; Dolgun, Z. Nihal; Gurkan, Hakan; Erzincan, Selen Gursoy; Uzun, Isil; Sutcu, Havva; Ates, Sinan; Atli, Emine; Varol, Fusun Journal: Journal of maternal-fetal & neonatal medicine Issue: Volume 32:Number 10(2019) Page Start: 1688 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
15. Relationship between arginase genes polymorphisms and preschool wheezing phenotypes. Issue 2 (23rd December 2020) Authors: Gokmirza Ozdemir, Pinar; Eker, Damla; Celik, Velat; Beken, Burcin; Gurkan, Hakan; Yazicioglu, Mehtap; Sut, Necdet Journal: Pediatric pulmonology Issue: Volume 56:Issue 2(2021) Page Start: 561 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
16. Schizencephaly accompanied by occipital encephalocele and deletion of chromosome 22q13.32: a case report. (2nd November 2019) Authors: Inan, Cihan; Sayin, N. Cenk; Gurkan, Hakan; Atli, Engin; Gursoy Erzincan, Selen; Uzun, Isil; Sutcu, Havva; Dogan, Sumeyra; Ikbal Atli, Emine; Varol, Fusun Journal: Fetal and pediatric pathology Issue: Volume 38:Number 6(2019) Page Start: 496 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
17. Screening for Y Chromosome Microdeletion in a Nonobstructive Azoospermic Male Patient with Allogeneic Bone Marrow Transplantation from His Sister. (5th December 2010) Authors: Gurkan, Hakan; Kucukdurmaz, Faruk; Akman, Tolga; Aydın, Filiz; Kadioglu, Ates Other Names: de Carvalho Mamede Academic Editor. Journal: Case reports in medicine Issue: Volume 2010(2010) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
18. Targeted next-generation sequencing as a diagnostic tool in gastrointestinal system cancer/polyposis patients. Issue 6 (December 2020) Authors: Yalcintepe, Sinem; Gurkan, Hakan; Demir, Selma; Tozkir, Hilmi; Tezel, Huseyin Ahmet; Atli, Emine Ikbal; Atli, Engin; Eker, Damla; Cicin, Irfan Journal: Tumori Issue: Volume 106:Issue 6(2020) Page Start: 510 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
19. Tetrasomy 18p in a Twin Pregnancy with Diverse Expression in Both Fetuses. (2nd September 2016) Authors: Inan, Cihan; Sayın, N. Cenk; Atlı, Emine; Ulusal, Selma; Erzincan, Selen; Uzun, Isil; Gurkan, Hakan; Varol, Füsun G. Journal: Fetal and pediatric pathology Issue: Volume 35:Number 5(2016) Page Start: 339 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
20. The Effect of TGFB1 and CD14 Gene Polymorphisms on the Clinical Findings of Cystic Fibrosis in Turkish Patients. (1st March 2016) Authors: Temurhan, Sonay; Tamay, Zeynep; Gurkan, Hakan; Akgul, Sebahat; Ozceker, Deniz; Kekik, Cigdem; Cagatay, Penbe; Aydin, Filiz; Guler, Nermin Journal: International journal of human genetics Issue: Volume 16:Number 1/2(2016) Page Start: 40 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗