1. Alu element insertion in the MLH1 exon 6 coding sequence as a mutation predisposing to Lynch syndrome. Issue 6 (21st May 2019) Authors: Solassol, Jérôme; Larrieux, Marion; Leclerc, Julie; Ducros, Vincent; Corsini, Carole; Chiésa, Jean; Pujol, Pascal; Rey, Jean‐Marc Journal: Human mutation Issue: Volume 40:Issue 6(2019) Page Start: 716 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗