1. A role for TENM1 mutations in congenital general anosmia. Issue 3 (31st May 2016) Authors: Alkelai, A.; Olender, T.; Haffner‐Krausz, R.; Tsoory, M.M.; Boyko, V.; Tatarskyy, P.; Gross‐Isseroff, R.; Milgrom, R.; Shushan, S.; Blau, I.; Cohn, E.; Beeri, R.; Levy-Lahad, E.; Pras, E.; Lancet, D. Journal: Clinical genetics Issue: Volume 90:Issue 3(2016) Page Start: 211 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Exome sequencing as a differential diagnosis tool: resolving mild trichohepatoenteric syndrome. (21st October 2014) Authors: Oz‐Levi, D.; Weiss, B.; Lahad, A.; Greenberger, S.; Pode‐Shakked, B.; Somech, R.; Olender, T.; Tatarsky, P.; Marek‐Yagel, D.; Pras, E.; Anikster, Y.; Lancet, D. Journal: Clinical genetics Issue: Volume 87:Number 6(2015:Jun.) Page Start: 602 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗