1. Reassessing the clinical spectrum associated with hereditary leiomyomatosis and renal cell carcinoma syndrome in French FH mutation carriers. Issue 6 (2nd May 2017) Authors: Muller, M.; Ferlicot, S.; Guillaud‐Bataille, M.; Le Teuff, G.; Genestie, C.; Deveaux, S.; Slama, A.; Poulalhon, N.; Escudier, B.; Albiges, L.; Soufir, N.; Avril, M.‐F.; Gardie, B.; Saldana, C.; Allory, Y.; Gimenez‐Roqueplo, A.‐P.; Bressac‐de Paillerets, B.; Richard, S.; Benusiglio, P.R. Journal: Clinical genetics Issue: Volume 92:Issue 6(2017) Page Start: 606 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗