1. Comparative genomic hybridisation shows a partial de novo deletion 16p11.2 in a neonate with multiple congenital malformations. Issue 5 (1st May 2002) Authors: Hernando, C; Plaja, A; Rigola, M A; Pérez, M M; Vendrell, T; Egocue, J; Fuster, C Journal: Journal of medical genetics Issue: Volume 39:Issue 5(2002) Page Start: e24 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗