1. Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation. Issue 2 (1st June 2005) Authors: Donaudy, F; Zheng, L; Ficarella, R; Ballana, E; Carella, M; Melchionda, S; Estivill, X; Bartles, J R; Gasparini, P Journal: Journal of medical genetics Issue: Volume 43:Issue 2(2006) Page Start: 157 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. International workshop on molecular genetics of haemochromatosis, held at Villa Feltrinelli, Gargnano (Bs), Italy, 25 September 1994. Issue 4 (April 1995) Authors: Worwood, M; Gasparini, P; Camaschella, C Journal: Journal of medical genetics Issue: Volume 32:Issue 4(1995) Page Start: 320 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. LTF and DEFB1 polymorphisms are associated with susceptibility toward chronic periodontitis development. (5th June 2017) Authors: Zupin, L; Robino, A; Navarra, CO; Pirastu, N; Di Lenarda, R; Gasparini, P; Crovella, S; Bevilacqua, L Journal: Oral diseases Issue: Volume 23:Number 7(2017) Page Start: 1001 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. 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) ↗
5. Pancreatic function and gene deletion F508 in cystic fibrosis. Issue 11 (November 1990) Authors: Borgo, G; Mastella, G; Gasparini, P; Zorzanello, A; Doro, R; Pignatti, P F Journal: Journal of medical genetics Issue: Volume 27:Issue 11(1990) Page Start: 665 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. RET fusions in a small subset of advanced colorectal cancers at risk of being neglected. (10th March 2018) Authors: Pietrantonio, F; Di Nicolantonio, F; Schrock, A B; Lee, J; Morano, F; Fucà, G; Nikolinakos, P; Drilon, A; Hechtman, J F; Christiansen, J; Gowen, K; Frampton, G M; Gasparini, P; Rossini, D; Gigliotti, C; Kim, S T; Prisciandaro, M; Hodgson, J; Zaniboni, A; Chiu, V K Journal: Annals of oncology Issue: Volume 29:Number 6(2018) Page Start: 1394 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. The genotype of a new linked DNA marker, MP6d-9, is related to the clinical course of cystic fibrosis. Issue 1 (January 1990) Authors: Gasparini, P; Novelli, G; Estivill, X; Olivieri, D; Savoia, A; Ruzzo, A; Nunes, V; Borgo, G; Antonelli, M; Williamson, R Journal: Journal of medical genetics Issue: Volume 27:Issue 1(1990) Page Start: 17 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Usher syndrome type III (USH3) linked to chromosome 3q in an Italian family. Issue 8 (August 1998) Authors: Gasparini, P; De Fazio, A; Croce, A I; Stanziale, P; Zelante, L Journal: Journal of medical genetics Issue: Volume 35:Issue 8(1998) Page Start: 666 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗