Browsing by Author Düzcan, F.
Showing results 1 to 5 of 5
| Issue Date | Title | Author(s) |
|---|---|---|
| 2020 | A Case Of Recombinant Chromosome 4: Further Delineation Of The Clinical Features | Anlaş, Ö.; Çetin, G.O.; Yararbaş, K.; Düzcan, F.; Gunduz, C.N.S.; Ayaz, A.; Bağcı, G. |
| 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 | 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. |