1. A locus for primary ciliary dyskinesia maps to chromosome 19q. Issue 4 (1st April 2000) Authors: Meeks, M; Walne, A; Spiden, S; Simpson, H; Mussaffi-Georgy, H; Hamam, H D; Fehaid, E L; Cheehab, M; Al-Dabbagh, M; Polak-Charcon, S; Blau, H; O'Rawe, A; Mitchison, H M; Gardiner, R M; Chung, E Journal: Journal of medical genetics Issue: Volume 37:Issue 4(2000) Page Start: 241 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Rapid diagnostic test for the major mutation underlying Batten disease. Issue 12 (December 1996) Authors: Järvelä, I; Mitchison, H M; Munroe, P B; O'Rawe, A M; Mole, S E; Syvänen, A C Journal: Journal of medical genetics Issue: Volume 33:Issue 12(1996) Page Start: 1041 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Sharing of PPT mutations between distinct clinical forms of neuronal ceroid lipofuscinoses in patients from Scotland. Issue 9 (September 1998) Authors: Munroe, P B; Greene, N D; Leung, K Y; Mole, S E; Gardiner, R M; Mitchison, H M; Stephenson, J B; Crow, Y J Journal: Journal of medical genetics Issue: Volume 35:Issue 9(1998) Page Start: 790 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗