| Issue Date | Title | Author(s) |
| 2018 | Co-existence of goldenhar and klinefelter syndromes in a patient born following ICSI | Zeybek, S.; Sarıkepe, B.; Bağcı, Gülseren ; Alataş, E. ; Düzcan, F. |
| 2003 | Familial Pericentric Inversion: Inv(4)(p16q12) | Bal, F.; Düzcan, F.; Atmaca, M.; Balci, A. |
| 2003 | Family history, clinical features, and molecular characterization of a patient with autosomal recessive non-syndromic hearing loss | Düzcan, F.; Wollnik, B.; Tepeli, E.; Ardıç, Fazıl Necdet ; Uyguner, O.; Bağcı, Hüseyin. |
| 2004 | Femoral-facial syndrome with hemifacial microsomia and hypoglossia | Düzcan, F.; Ergin, H. ; Perçin, E.F.; Tepeli, E.; Erkula, G. |
| 2015 | A Newborn with Congenital Mixed Phenotype Acute Leukemia After In Vitro Fertilization | Ergin, Hacer. ; Özdemir, Özmert Muhamet Ali ; Karaca, A.; Türk, Nilay Şen ; Düzcan, F.; Ergin, Ş.; Kazanci, E. |
| 2009 | De novo partial trisomy of the subtelomeric region of 1q on 1pter causing dysmorphic features | Düzcan, F.; Çetin, G.; Kalkan, T.; Erdogan, K; Semiz, S. |
| 2006 | Ovarian agenesis and MURCS association | Yildirim, B.; Semerci, C.N.; Ya?ci, B.; Duman, K.; Düzcan, F. |
