1. A novel heterozygous IGF-1 receptor mutation associated with hypoglycemia. Issue 6 (August 2017) Authors: Solomon-Zemler, R; Basel-Vanagaite, L; Steier, D; Yakar, S; Mel, E; Phillip, M; Bazak, L; Bercovich, D; Werner, H; de Vries, L Journal: Endocrine connections Issue: Volume 6:Issue 6(2017) Page Start: 395 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation. Issue 3 (20th July 2005) Authors: Basel-Vanagaite, L; Attia, R; Yahav, M; Ferland, R J; Anteki, L; Walsh, C A; Olender, T; Straussberg, R; Magal, N; Taub, E; Drasinover, V; Alkelai, A; Bercovich, D; Rechavi, G; Simon, A J; Shohat, M Journal: Journal of medical genetics Issue: Volume 43:Issue 3(2006) Page Start: 203 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗