1. A microdeletion in 19q13.2 associated with mental retardation, skeletal malformations, and Diamond-Blackfan anaemia suggests a novel contiguous gene syndrome. Issue 2 (1st February 2000) Authors: Tentler, Dmitry; Gustavsson, Peter; Elinder, Göran; Eklöf, Ole; Gordon, Laurie; Mandel, Ariane; Dahl, Niklas Journal: Journal of medical genetics Issue: Volume 37:Issue 2(2000) Page Start: 128 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗