1. Clinical and molecular characterization of Rubinstein‐Taybi syndrome patients carrying distinct novel mutations of the EP300 gene. (17th February 2014) Authors: Negri, G.; Milani, D.; Colapietro, P.; Forzano, F.; Della Monica, M.; Rusconi, D.; Consonni, L.; Caffi, L. G.; Finelli, P.; Scarano, G.; Magnani, C.; Selicorni, A.; Spena, S.; Larizza, L.; Gervasini, C. Journal: Clinical genetics Issue: Volume 87:Number 2(2015:Feb.) Page Start: 148 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Clinical and molecular characterization of two patients with palmoplantar keratoderma–congenital alopecia syndrome type 2. (1st August 2016) Authors: Castori, M.; Morlino, S.; Sana, M. E.; Paradisi, M.; Tadini, G.; Angioni, A.; Malacarne, M.; Grammatico, P.; Iascone, M.; Forzano, F. Journal: Clinical and experimental dermatology Issue: Volume 41:Number 6(2016) Page Start: 632 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Clinical and molecular characterization of two patients with palmoplantar keratoderma–congenital alopecia syndrome type 2. (24th June 2016) Authors: Castori, M.; Morlino, S.; Sana, M. E.; Paradisi, M.; Tadini, G.; Angioni, A.; Malacarne, M.; Grammatico, P.; Iascone, M.; Forzano, F. Journal: Clinical and experimental dermatology Issue: Volume 41:Number 6(2016) Page Start: 632 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗