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) ↗
2. Novel founder mutation in French‐Canadian families with Naxos disease. Issue 4 (22nd February 2017) Authors: Marino, T. Cruz; Maranda, B.; Leblanc, J.; Pratte, A.; Barabas, M.; Dupéré, A.; Lévesque, S. Journal: Clinical genetics Issue: Volume 92:Issue 4(2017) Page Start: 451 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗