1. Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17. Issue 9 (September 1991) Authors: Koch, M C; Ricker, K; Otto, M; Grimm, T; Hoffman, E P; Rüdel, R; Bender, K; Zoll, B; Harper, P S; Lehmann-Horn, F Journal: Journal of medical genetics Issue: Volume 28:Issue 9(1991) Page Start: 583 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1). Issue 3 (September 1994) Authors: Jardine, P E; Koch, M C; Lunt, P W; Maynard, J; Bathke, K D; Harper, P S; Upadhyaya, M Journal: Archives of disease in childhood Issue: Volume 71:Issue 3(1994) Page Start: 221 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Evidence for genetic homogeneity in autosomal recessive generalised myotonia (Becker). Issue 11 (November 1993) Authors: Koch, M C; Ricker, K; Otto, M; Wolf, F; Zoll, B; Lorenz, C; Steinmeyer, K; Jentsch, T J Journal: Journal of medical genetics Issue: Volume 30:Issue 11(1993) Page Start: 914 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Human T and risk for neural tube defects. Issue 3 (1st March 2002) Authors: Richter, B; Schultealbert, A H; Koch, M C Journal: Journal of medical genetics Issue: Volume 39:Issue 3(2002) Page Start: e14 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗