1. Characterization of a novel founder MSH6 mutation causing Lynch syndrome in the French Canadian population. (22nd November 2014) Authors: Castellsagué, E.; Liu, J.; Volenik, A.; Giroux, S.; Gagné, R.; Maranda, B.; Roussel‐Jobin, A.; Latreille, J.; Laframboise, R.; Palma, L.; Kasprzak, L.; Marcus, V.A.; Breguet, M.; Nolet, S.; El‐Haffaf, Z.; Australie, K.; Gologan, A.; Aleynikova, O.; Oros‐Klein, K.; Greenwood, C. Journal: Clinical genetics Issue: Volume 87:Number 6(2015:Jun.) Page Start: 536 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗