Browsing by Subject Abnormalities, Multiple
Showing results 1 to 8 of 8
| Issue Date | Title | Author(s) |
|---|---|---|
| 2014 | An adolescent diagnosed with double aortic arch | Fırıncı, Fatih ; Akpınar, Funda ; Aslan, Sema Yıldırım; Doğan, Mustafa ; Koçyiğit, Ali ; Mete, Emin |
| 2007 | Association of rare intestinal malformations: Colonic atresia and intestinal neuronal dysplasia | Çördük, Nurgül ; Koltuksuz, Uğur ; Bir, Ferda. ; Karabul, Murat ; Herek, Özkan. ; Sarıoğlu-Buke, Akile |
| 1998 | Camptodactyly, myopia, and fibrosis of the medial rectus of the eye in two sibs born to consanguineous parents: Autosomal recessive entity? | Kılıç, İlknur ; Kılıç, B. Alper ; Ergin, Hacer ; Aygün, M.G.; Akşit, M. Arif |
| 2006 | A case with proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H) associated with urogenital anomalies | Ergin, Hacer ; Semerci, Cavidan Nur ; Bican, M.; Düzcan, Füsun ; Yagci, A.B. ; Erdogan, K.M.; Tufan, Ahmet Çevik |
| 2008 | Congenital lymphoedema, bronchiectasis and seizure: Case report | Semiz, Serap ; Dagdeviren, E.; Ergin, H. ; Kilic, I.; Kirac, S. ; Cimbis, M.; Semiz, E. |
| 2004 | Femoral-facial syndrome with hemifacial microsomia and hypoglossia | Düzcan, F.; Ergin, H. ; Perçin, E.F.; Tepeli, E. ; Erkula, G. |
| 2008 | Multidetector Computed Tomographic Angiography Findings in a Rare Case of Popliteal Artery Entrapment Syndrome | Öztoprak, I.; Gümüş, C.; Egilmez, H.; Manduz, S.; Öztoprak, B.; Emrecan, B. |
| 2012 | Terminal 14q deletion with unbalanced t(Y;14)(q12;q32) translocation | Bagcı, Gülseren ; Çetin, Gökhan Ozan ; Semerci, Nur ; Toruner, G. A.; Cinbiş, Mine |