1. A clinical, cytogenetic, and molecular study of 40 adults with the Prader-Willi syndrome. Issue 3 (March 1995) Authors: Webb, T; Clarke, D; Hardy, C A; Kilpatrick, M W; Corbett, J; Dahlitz, M Journal: Journal of medical genetics Issue: Volume 32:Issue 3(1995) Page Start: 181 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Adrenoleucodystrophy: a molecular genetic study in five families. Issue 11 (November 1990) Authors: Del Mastro, R G; Bundey, S; Kilpatrick, M W Journal: Journal of medical genetics Issue: Volume 27:Issue 11(1990) Page Start: 670 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. An exclusion map of Marfan syndrome. Issue 2 (February 1990) Authors: Blanton, S H; Sarfarazi, M; Eiberg, H; de Groote, J; Farndon, P A; Kilpatrick, M W; Child, A H; Pope, F M; Peltonen, L; Francomano, C A Journal: Journal of medical genetics Issue: Volume 27:Issue 2(1990) Page Start: 73 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Possible genetic heterogeneity in hypochondroplasia. Issue 6 (June 1995) Authors: Stoilov, I; Kilpatrick, M W; Tsipouras, P; Costa, T Journal: Journal of medical genetics Issue: Volume 32:Issue 6(1995) Page Start: 492 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. X linked exudative vitreoretinopathy: clinical features and genetic linkage analysis. Issue 3 (March 1993) Authors: Fullwood, P; Jones, J; Bundey, S; Dudgeon, J; Fielder, A R; Kilpatrick, M W Journal: British journal of ophthalmology Issue: Volume 77:Issue 3(1993) Page Start: 168 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗