1. Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndrome. Issue 10 (October 1996) Authors: Horsthemke, B; Maat-Kievit, A; Sleegers, E; van den Ouweland, A; Buiting, K; Lich, C; Mollevanger, P; Beverstock, G; Gillessen-Kaesbach, G; Schwanitz, G Journal: Journal of medical genetics Issue: Volume 33:Issue 10(1996) Page Start: 848 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Paradox of a better test for Huntington's disease. Issue 5 (1st November 2000) Authors: Maat-Kievit, A; Vlis, M Vegter-van der; Zoeteweij, M; Losekoot, M; van Haeringen, A; Roos, R Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 69:Issue 5(2000) Page Start: 579 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗