Browsing by Author Duzcan, F
Showing results 1 to 4 of 4
| Issue Date | Title | Author(s) |
|---|---|---|
| 2008 | A 12 years old boy with Prader-Willi syndrome and early onset diabetic nephropathy | Semiz, S; Candemir, M; Duzcan, F; Karaca, A |
| 1999 | Association of a rare fragile site 16q22 with Down syndrome in a patient and his mother | Duzcan, F; Bagci, H; Polat, A |
| 2009 | Prenatally diagnosed de novo inverted duplication of 8p11.2-p23 region with deletion of 8pter in a dysmorphic case | Cetin, G; Erdogan, K; Ozdemir, O; Kalkan, T; Kaleli, B ; Kilic, I; Duzcan, F |
| 2013 | Significance of Parental Karyotyping: Case Report | Zeybek, S; Cetin, O; Fenkci, V; Duzcan, F; Atmaca, M; Semerci, N; Bagci, G |