1. CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome. Issue 12 (24th September 2013) Authors: Brioude, F; Oliver-Petit, I; Blaise, A; Praz, F; Rossignol, S; Jule, M Le; Thibaud, N; Faussat, A-M; Tauber, M; Bouc, Y Le; Netchine, I Journal: Journal of medical genetics Issue: Volume 50:Issue 12(2013) Page Start: 823 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. The current landscape of European registries for rare endocrine conditions. Issue 1 (January 2019) Authors: Ali, S R; Bryce, J; Cools, M; Korbonits, M; Beun, J G; Taruscio, D; Danne, T; Dattani, M; Dekkers, O M; Linglart, A; Netchine, I; Nordenstrom, A; Patocs, A; Persani, L; Reisch, N; Smyth, A; Sumnik, Z; Visser, W E; Hiort, O; Pereira, A M Journal: European journal of endocrinology Issue: Volume 180:Issue 1(2019) Page Start: 89 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗