1. DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure. Issue 6 (December 1986) Authors: Bakker, E; Bonten, E J; De Lange, L F; Veenema, H; Majoor-Krakauer, D; Hofker, M H; Van Ommen, G J; Pearson, P L Journal: Journal of medical genetics Issue: Volume 23:Issue 6(1986) Page Start: 573 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutations. Issue 9 (September 1989) Authors: Bakker, E; Veenema, H; Den Dunnen, J T; van Broeckhoven, C; Grootscholten, P M; Bonten, E J; van Ommen, G J; Pearson, P L Journal: Journal of medical genetics Issue: Volume 26:Issue 9(1989) Page Start: 553 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗