1. Characterisation of heterozygous PMS2 variants in French patients with Lynch syndrome. Issue 7 (28th January 2020) Authors: Wang, Qing; Leclerc, Julie; Bougeard, Gaëlle; Olschwang, Sylviane; Vasseur, Stéphanie; Cassinari, Kévin; Boidin, Denis; Lefol, Cédrick; Naïbo, Pierre; Frébourg, Thierry; Buisine, Marie Pierre; Baert-Desurmont, Stéphanie Journal: Journal of medical genetics Issue: Volume 57:Issue 7(2020) Page Start: 487 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. MSH2 c.1022T>C, p.Leu341Pro is a founder pathogenic variation and a major cause of Lynch syndrome in the North of France. Issue 2 (3rd September 2019) Authors: Vermaut, Catherine; Leclerc, Julie; Vasseur, Francis; Wacrenier, Agnes; Lovecchio, Tonio; Boidin, Denis; Rebergue, Marie‐Helene; Cattan, Stephane; Manouvrier, Sylvie; Lejeune, Sophie; Buisine, Marie‐Pierre Journal: Genes, chromosomes & cancer Issue: Volume 59:Issue 2(2020) Page Start: 111 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗