1. CRIM1 haploinsufficiency causes defects in eye development in human and mouse. (5th January 2015) Authors: Beleggia, Filippo; Li, Yun; Fan, Jieqing; Elcioğlu, Nursel H.; Toker, Ebru; Wieland, Thomas; Maumenee, Irene H.; Akarsu, Nurten A.; Meitinger, Thomas; Strom, Tim M.; Lang, Richard; Wollnik, Bernd Journal: Human molecular genetics Issue: Volume 24:Number 8(2015:Apr. 15) Page Start: 2267 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Mutations in the interleukin receptor IL11RA cause autosomal recessive Crouzon‐like craniosynostosis. Issue 4 (19th August 2013) Authors: Keupp, Katharina; Li, Yun; Vargel, Ibrahim; Hoischen, Alexander; Richardson, Rebecca; Neveling, Kornelia; Alanay, Yasemin; Uz, Elif; Elcioğlu, Nursel; Rachwalski, Martin; Kamaci, Soner; Tunçbilek, Gökhan; Akin, Burcu; Grötzinger, Joachim; Konas, Ersoy; Mavili, Emin; Müller‐Newen, Gerhard; Collman... Journal: Molecular genetics & genomic medicine Issue: Volume 1:Issue 4(2013:Nov.) Page Start: 223 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗