1. Expanding the MYBPC1 phenotypic spectrum: a novel homozygous mutation causes arthrogryposis multiplex congenita. Issue 1 (20th January 2016) Authors: Ekhilevitch, N.; Kurolap, A.; Oz‐Levi, D.; Mory, A.; Hershkovitz, T.; Ast, G.; Mandel, H.; Baris, H.N. Journal: Clinical genetics Issue: Volume 90:Issue 1(2016) Page Start: 84 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Genetic features of Lynch syndrome in the Israeli population. (28th November 2014) Authors: Goldberg, Y.; Barnes‐Kedar, I.; Lerer, I.; Halpern, N.; Plesser, M.; Hubert, A.; Kadouri, L.; Goldshmidt, H.; Solar, I.; Strul, H.; Rosner, G.; Baris, H.N.; Peretz, T.; Levi, Z.; Kariv, R. Journal: Clinical genetics Issue: Volume 87:Number 6(2015:Jun.) Page Start: 549 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. The gastrointestinal manifestation of constitutional mismatch repair deficiency syndrome: from a single adenoma to polyposis‐like phenotype and early onset cancer. (10th November 2014) Authors: Levi, Z.; Kariv, R.; Barnes‐Kedar, I.; Goldberg, Y.; Half, E.; Morgentern, S.; Eli, B.; Baris, H.N.; Vilkin, A.; Belfer, R.G.; Niv, Y.; Elhasid, R.; Dvir, R.; Abu‐Freha, N.; Cohen, S. Journal: Clinical genetics Issue: Volume 88:Number 5(2015:Nov.) Page Start: 474 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗