1. A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation. (2019) Authors: Jaouadi, Hager; Chehida, Amel Ben; Kraoua, Lilia; Etchevers, Heather C.; Argiro, Laurent; Kasdallah, Nadia; Blibech, Sonia; Delague, Valérie; Lévy, Nicolas; Tebib, Néji; Mrad, Ridha; Abdelhak, Sonia; Benkhalifa, Rym; Zaffran, Stéphane Journal: Genetical research Issue: Volume 101(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation. (29th April 2019) Authors: Jaouadi, Hager; Chehida, Amel Ben; Kraoua, Lilia; Etchevers, Heather C.; Argiro, Laurent; Kasdallah, Nadia; Blibech, Sonia; Delague, Valérie; Lévy, Nicolas; Tebib, Néji; Mrad, Ridha; Abdelhak, Sonia; Benkhalifa, Rym; Zaffran, Stéphane Journal: Genetical research Issue: Volume 101(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗