| Effects of indoleamines on sperm motility in vitro TÖ Irez, H Senol, M Alagöz, C Basmaciogullari, F Turan, D Kuru, ... Human Reproduction 7 (7), 987-990, 1992 | 29 | 1992 |
| Structural chromosomal abnormalities in couples with recurrent pregnancy loss A ÇIRAKOĞLU, Ş Yilmaz, D Kuru, YT ARGÜDEN, GS Güven, A Deviren, ... Turkiye klinikleri journal of medical sciences 30 (4), 1185-1188, 2010 | 11 | 2010 |
| Variant Philadelphia translocations with different breakpoints in six chronic myeloid leukemia patients D Kuru, Y Tarkan-Argüden, MC Ar, A Çırakoğlu, Ş Öngören, Ş Yılmaz, ... Turk J Haematol 28, 186-192, 2011 | 7 | 2011 |
| Cytogenetic clonal evolution in patients with chronic myeloid leukemia Y Tarkan-Arguden, MC Ar, S Yilmaz, S Ongoren, D Kuru, U Ure, ... Biotechnology & Biotechnological Equipment 23 (4), 1515-1520, 2009 | 5 | 2009 |
| Cytogenetic Evaluation in 221 Untreated Patients with Myelodysplastic Syndrome/Tedavi Almamis 221 Miyelodisplastik Sendromlu Hastada Sitogenetik Degerlendirme A Deviren, IMG Msc, SY Msc, S Hacihanefioglu Türkiye Klinikleri. Tip Bilimleri Dergisi 32 (1), 15, 2012 | 4 | 2012 |
| Clonal chromosomal abnormalities in Philadelphia-negative cells and their clinical significance in patients with chronic myeloid leukemia: results of a single center Ş ÖNGÖREN, YT ARGÜDEN, MC Ar, Ş YILMAZ, Ü ÜRE, D Kuru, ... Turkiye Klinikleri Journal of Medical Sciences 29 (2), 321-330, 2009 | 4 | 2009 |
| Supernumerary chromosome der (22) t (11; 22): Emanuel syndrome associates with novel features EY Fenerci, GS Guven, D Kuru, S Yilmaz, Y Tarkan-Argüden, A Cirakoglu, ... Genetic Counseling 18 (4), 401, 2007 | 4 | 2007 |
| Analysis of chromosome 3, 7 and 8 centromeric regions in bronchial lavage specimens by FISH S Atasoy, SS Erturan, N Yılmaz, D Kuru, A Çırakoğlu, Ş Yılmaz, A Deviren Turkish Thoracic Journal 17 (4), 141, 2016 | 3 | 2016 |
| Mosaic supernumerary r (8) syndrome S Yilmaz, Y Tarkan-Argüden, D Kuru, A Deviren, B Karaman, A Yüksel, ... Genetic counseling (Geneva, Switzerland) 16 (2), 187-190, 2005 | 3 | 2005 |
| Akut lenfoblastik lösemili hastalarda MYC gen bölgesindeki yeniden düzenlenmelerin konvansiyonel sitogenetik ve floresan in situ hibridizasyon yöntemleriyle incelenmesi E Seda, A ÇIRAKOĞLU, K Dilhan, Z Başlar, Ö Devecioğlu, M NALÇACI, ... Journal of Clinical and Experimental Investigations 6 (1), 21-26, 2015 | 1 | 2015 |
| Case Report Two Siblings with Currarino Syndrome with 7q34 Deletion Due to Maternal t (7; 14)(q34; p13) 母親帶基因 t (7; 14)(q34; p13) 導致兩兄弟 7q34 缺失患有 Currarino 綜合徵 Ş Yildirim, N Topaloğlu, F Silan, D Kuru HK J Paediatr (new series) 19 (3), 181-184, 2014 | 1 | 2014 |
| A childhood acute lymphoblastic leukemia (ALL) case with t (3; 17)(q23; p13), t (5; 12)(q31; p13), inv (11)(p15q12) D Kuru, F Yılmaz, SG Berra, C Canpolat, S Hacıhanefioğlu, YT Argüden, ... | 1 | 2008 |
| WITH UPDATE ON KARYOTYPES ANOMALIES EVALUATION AS RETROSPECTIVE OBSERVED IN POLYCYTHEMIA VERA DIAGNOSIS AND PREDIAGNOSIS CASES H Sahin, S Yilmaz, A Cirakoglu, D Kuru, A Salihoglu, S Berk, A Deviren, ... THROMBOSIS RESEARCH 141, S22-S22, 2016 | | 2016 |
| Recurrent Monosomies Confirmed by Interphase FISH in Three Chronic Myeloid Leukemia Cases YT Argüden, D Kuru, A Çırakoğlu, Ş Yılmaz, ŞÖ Aydın, CM Ar, A Deviren, ... Turkish Journal of Hematology 32 (1), 82, 2015 | | 2015 |
| Two Siblings with Currarino Syndrome with 7q34 Deletion Due to Maternal t (7; 14)(q34; p13) N Topaloglu, D Kuru, F SILAN, S Yildirim | | 2014 |
| Altı Kronik miyeloid lösemi olgusunda farklı kırık noktalı varyant Philadelphia translokasyonları D Kuru, Y Tarkan Argüden, MC Ar, A Çırakoğlu, Ş Öngören, Ş Yılmaz, ... | | 2011 |
| A childhood acute lymphoblastic leukemia (ALL) case with t (3; 17)(q23; p13), t (5; 12)(q31; p13), inv (11)(p15q12)/t (3; 17)(q23; p13), t (5; 12)(q31; p13), inv (11)(p15q12 … A Cirakoglu, Y Tarkan-Arguden, A Deviren, D Kuru, S Yilmaz, SG Berrak, ... Turkish Journal of Hematology, 152-155, 2008 | | 2008 |
| A childhood acute lymphoblastic leukemia (ALL) case with t (3; 17)(q23; p13), t (5; 12)(q31; p13), inv (11)(p15q12). A Çırakoğlu, Y Tarkan-Argüden, A Deviren, D Kuru, Ş Yılmaz, ... Turkish Journal of Hematology 25 (3), 2008 | | 2008 |
| Two sibs with currarino syndrome with 7q34 deletion due to maternal t (7; 14)(q34; p13) Silan, C Zafer, D Kuru, K Mahmutyazicioglu, S Hacihanefioglu CHROMOSOME RESEARCH 15, 120-120, 2007 | | 2007 |
| Structural chromosome abnormalities in couples with recurrent fetal losses Y Cirakoglu, S Yilmaz, D Kuru, A Deviren, GS Guven, E Pasalioglu, ... CHROMOSOME RESEARCH 15, 103-103, 2007 | | 2007 |
