1. Homozygous indel mutation in CDH11 as the probable cause of Elsahy–Waters syndrome. Issue 12 (8th October 2017) Authors: Taskiran, Ekim Z.; Karaosmanoglu, Beren; Koşukcu, Can; Doğan, Özlem A.; Taylan‐Şekeroğlu, Hande; Şimşek‐Kiper, Pelin Ö.; Utine, Eda G.; Boduroğlu, Koray; Alikaşifoğlu, Mehmet Journal: American journal of medical genetics Issue: Volume 173:Issue 12(2017) Page Start: 3143 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗