Browsing by Author Cinbis, M.
Showing results 1 to 5 of 5
| Issue Date | Title | Author(s) |
|---|---|---|
| 2005 | Association of homozygote pericentric inversion of chromosome 7 (inv(7)(p11.2q22)) with autosomal recessive lissencephaly and RELN mutation | Düzcan, Füsun ; Chang, B. S.; Cinbis, M.; Ozdel, O. ; Atmaca, M.; Zencir, S.; Kim, S. |
| 2009 | Dandy-Walker's variant and tetralogy of Fallot with atrial septal defect and patent ductus arteriosus and primary hypothyroidy - A new association | Özdemir, Özmert Muhammet Ali ; Polat, A.; Cinbis, M.; Kurt, F.; Kucuktasci, K.; Kiroglu, Y. |
| 2006 | Molecular genetic analyses in neurofibromatosis type 1 patients with tumors | Oguzkan, S.; Terzi, Y.K.; Cinbis, M.; Anlar, B.; Aysun, S.; Ayter, S. |
| 2005 | The Role of Brain Perfusion Scintigraphy in the Management of Patients with Viral Encephalitis | Yuksel, D. ; Cinbis, M.; Degirmencioglu, B.; Serdas, T.; Akalin, N.; Kirac, F. S. |
| 2007 | The role of RELN in lissencephaly and neuropsychiatric disease | Chang, B.S.; Düzcan, Füsun ; Kim, S.; Cinbis, M.; Aggarwal, A.; Apse, K.A.; Özdel, Osman İsmail |