1. Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinism. Issue 10 (October 1993) Authors: Meindl, A; Hosenfeld, D; Brückl, W; Schuffenhauer, S; Jenderny, J; Bacskulin, A; Oppermann, H C; Swensson, O; Bouloux, P; Meitinger, T Journal: Journal of medical genetics Issue: Volume 30:Issue 10(1993) Page Start: 838 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗