1. Molecular analysis of patients of Sardinian descent with Crigler-Najjar syndrome type I. Issue 2 (February 1997) Authors: Rosatelli, M C; Meloni, A; Faa, V; Saba, L; Crisponi, G; Clemente, M G; Meloni, G; Piga, M T; Cao, A Journal: Journal of medical genetics Issue: Volume 34:Issue 2(1997) Page Start: 122 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease. Issue 10 (19th September 2011) Authors: Uusimaa, J; Jungbluth, H; Fratter, C; Crisponi, G; Feng, L; Zeviani, M; Hughes, I; Treacy, E P; Birks, J; Brown, G K; Sewry, C A; McDermott, M; Muntoni, F; Poulton, J Journal: Journal of medical genetics Issue: Volume 48:Issue 10(2011) Page Start: 660 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. X-mapping in man: evidence against measurable linkage between anhidrotic ectodermal dysplasia and G6PD deficiency. Issue 3 (June 1979) Authors: Filippi, G; Rinaldi, A; Crisponi, G; Daniels, G L; Siniscalco, M Journal: Journal of medical genetics Issue: Volume 16:Issue 3(1979) Page Start: 223 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗