11. Analysis of GLRA1 in hereditary and sporadic hyperekplexia: a novel mutation in a family cosegregating for hyperekplexia and spastic paraparesis. Issue 5 (May 1996) Authors: Elmslie, F V; Hutchings, S M; Spencer, V; Curtis, A; Covanis, T; Gardiner, R M; Rees, M Journal: Journal of medical genetics Issue: Volume 33:Issue 5(1996) Page Start: 435 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
12. Association of less common cystic fibrosis mutations with a mild phenotype. Issue 1 (January 1991) Authors: Curtis, A; Nelson, R; Porteous, M; Burn, J; Bhattacharya, S S Journal: Journal of medical genetics Issue: Volume 28:Issue 1(1991) Page Start: 34 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
13. Confirmation of prenatal diagnosis of cystic fibrosis by DNA typing of fetal tissues. Issue 2 (February 1988) Authors: Curtis, A; Strain, L; Mennie, M; Brock, D J Journal: Journal of medical genetics Issue: Volume 25:Issue 2(1988) Page Start: 79 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
14. Enhanced electron acceleration in aligned nanowire arrays irradiated at highly relativistic intensities. (1st November 2019) Authors: Moreau, A; Hollinger, R; Calvi, C; Wang, S; Wang, Y; Capeluto, M G; Rockwood, A; Curtis, A; Kasdorf, S; Shlyaptsev, V N; Kaymak, V; Pukhov, A; Rocca, J J Journal: Plasma physics and controlled fusion Issue: Volume 62:Number 1(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
15. Experimental design for fully nonlinear source location problems: which method should I choose?. Issue 2 (29th July 2020) Authors: Bloem, H; Curtis, A; Maurer, H Journal: Geophysical journal international Issue: Volume 223:Issue 2(2020) Page Start: 944 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
16. Genetic heterogeneity in hereditary haemorrhagic telangiectasia. Issue 12 (December 1994) Authors: Porteous, M E; Curtis, A; Williams, O; Marchuk, D; Bhattacharya, S S; Burn, J Journal: Journal of medical genetics Issue: Volume 31:Issue 12(1994) Page Start: 925 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
17. Imaging strategies using focusing functions with applications to a North Sea field. Issue 1 (26th December 2017) Authors: da Costa Filho, C A; Meles, G A; Curtis, A; Ravasi, M; Kritski, A Journal: Geophysical journal international Issue: Volume 213:Issue 1(2018:Apr.) Page Start: 561 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
18. IMPACT OF NON-CARDIOVASCULAR COMORBIDITIES ON SHORT-TERM OUTCOMES AMONG OLDER ADULTS HOSPITALIZED FOR ACS. (16th November 2018) Authors: Ofori-Asenso, R; Zomer, E; Chin, K; Si, S; Ademi, Z; Curtis, A; Zoungas, S; Liew, D Journal: Innovation in aging Issue: Volume 2(2018)Supplement 1 Page Start: 951 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
19. Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 1. Trends across the clinical groups. Issue 9 (September 1993) Authors: Nicholson, L V; Johnson, M A; Bushby, K M; Gardner-Medwin, D; Curtis, A; Ginjaar, I B; den Dunnen, J T; Welch, J L; Butler, T J; Bakker, E Journal: Journal of medical genetics Issue: Volume 30:Issue 9(1993) Page Start: 728 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
20. Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 2. Correlations within individual patients. Issue 9 (September 1993) Authors: Nicholson, L V; Johnson, M A; Bushby, K M; Gardner-Medwin, D; Curtis, A; Ginjaar, I B; den Dunnen, J T; Welch, J L; Butler, T J; Bakker, E Journal: Journal of medical genetics Issue: Volume 30:Issue 9(1993) Page Start: 737 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗