1. Familial schizencephaly: further delineation of a rare disorder. Issue 3 (March 1995) Authors: Haverkamp, F; Zerres, K; Ostertun, B; Emons, D; Lentze, M J Journal: Journal of medical genetics Issue: Volume 32:Issue 3(1995) Page Start: 242 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Interstitial deletion in Xp22.3 is associated with X linked ichthyosis, mental retardation, and epilepsy. Issue 8 (1st August 2000) Authors: Gohlke, B C; Haug, K; Fukami, M; Friedl, W; Noeker, M; Rappold, G A; Haverkamp, F Journal: Journal of medical genetics Issue: Volume 37:Issue 8(2000) Page Start: 600 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗