1. Burkholderia cepacia and delta F508 homozygosity in cystic fibrosis. Issue 3 (September 1995) Authors: Castellani, C; Bonizzato, A; Cazzola, G A; Amalfitano, G; Mastella, G Journal: Archives of disease in childhood Issue: Volume 73:Issue 3(1995) Page Start: 276 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. CFTR mutations and IVS8-5T variant in newborns with hypertrypsinaemia and normal sweat test. Issue 4 (April 1997) Authors: Castellani, C; Bonizzato, A; Mastella, G Journal: Journal of medical genetics Issue: Volume 34:Issue 4(1997) Page Start: 297 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Nine cystic fibrosis patients homozygous for the CFTR nonsense mutation R1162X have mild or moderate lung disease. Issue 8 (August 1992) Authors: Gasparini, P; Borgo, G; Mastella, G; Bonizzato, A; Dognini, M; Pignatti, P F Journal: Journal of medical genetics Issue: Volume 29:Issue 8(1992) Page Start: 558 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗