1. A germline mutation in KIT in familial diffuse cutaneous mastocytosis. Issue 6 (1st June 2004) Authors: Tang, X; Boxer, M; Drummond, A; Ogston, P; Hodgins, M; Burden, A D Journal: Journal of medical genetics Issue: Volume 41:Issue 6(2004) Page Start: e88 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A linkage map of 10 loci flanking the Marfan syndrome locus on 15q: results of an International Consortium study. Issue 2 (February 1992) Authors: Sarfarazi, M; Tsipouras, P; Del Mastro, R; Kilpatrick, M; Farndon, P; Boxer, M; Bridges, A; Boileau, C; Junien, C; Hayward, C Journal: Journal of medical genetics Issue: Volume 29:Issue 2(1992) Page Start: 75 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Ascertainment and severity of Marfan syndrome in a Scottish population. Issue 1 (January 1994) Authors: Gray, J R; Bridges, A B; Faed, M J; Pringle, T; Baines, P; Dean, J; Boxer, M Journal: Journal of medical genetics Issue: Volume 31:Issue 1(1994) Page Start: 51 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Marfan syndrome in a large family: response of family members to a screening programme. Issue 2 (February 1992) Authors: Bridges, A B; Faed, M; Boxer, M; Gray, J R; Bundy, C; Murray, A Journal: Journal of medical genetics Issue: Volume 29:Issue 2(1992) Page Start: 81 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Muscle fibrillin deficiency in Marfan's syndrome myopathy. Issue 5 (1st May 2003) Authors: Behan, W M H; Longman, C; Petty, R K H; Comeglio, P; Child, A H; Boxer, M; Foskett, P; Harriman, D G F Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 74:Issue 5(2003) Page Start: 633 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Prenatal exclusion testing for Huntington's disease: a problem of too much information. Issue 2 (February 1989) Authors: Millan, F A; Curtis, A; Mennie, M; Holloway, S; Boxer, M; Faed, M J; Crawford, J W; Liston, W A; Brock, D J Journal: Journal of medical genetics Issue: Volume 26:Issue 2(1989) Page Start: 83 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗