1. A case with isochromosome 18p and 2q13 deletion including the BUB1 gene. Issue 3 (July 2018) Authors: Ayaz, Akif; Topak, Ali; Yalcintepe, Sinem; Celik, Tamer; Yararbas, Kanay; Eser, Metin; Yuregir, Ozge O. Journal: Clinical dysmorphology Issue: Volume 27:Issue 3(2018:Jul.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A Large PROP1 Gene Deletion in a Turkish Pedigree. (14th March 2018) Authors: Gorar, Suheyla; Turkkahraman, Doga; Yararbas, Kanay Other Names: Frindik J. Paul Academic Editor. Journal: Case reports in endocrinology Issue: Volume 2018(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. AUTS2 Syndrome in a 68‐year‐old female: Natural history and further delineation of the phenotype. Issue 12 (17th August 2016) Authors: Sengun, Ece; Yararbas, Kanay; Kasakyan, Serdar; Alanay, Yasemin Journal: American journal of medical genetics Issue: Volume 170:Issue 12(2016) Page Start: 3231 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Concomitant Alpha- and Gamma-Sarcoglycan Deficiencies in a Turkish Boy with a Novel Deletion in the Alpha-Sarcoglycan Gene. (22nd June 2014) Authors: Diniz, Gulden; Tosun Yildirim, Hulya; Gokben, Sarenur; Serdaroglu, Gul; Hazan, Filiz; Yararbas, Kanay; Tukun, Ajlan Other Names: Morrison Patrick Academic Editor. Journal: Case reports in genetics Issue: Volume 2014(2014) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗