1. Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?. (19th April 2013) Authors: Shoukier, M; Klein, N; Auber, B; Wickert, J; Schröder, J; Zoll, B; Burfeind, P; Bartels, I; Alsat, EA; Lingen, M; Grzmil, P; Schulze, S; Keyser, J; Weise, D; Borchers, M; Hobbiebrunken, E; Röbl, M; Gärtner, J; Brockmann, K; Zirn, B Journal: Clinical genetics Issue: Volume 83:Number 1(2013:Jan.) Page Start: 53 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?. (21st February 2012) Authors: Shoukier, M; Klein, N; Auber, B; Wickert, J; Schröder, J; Zoll, B; Burfeind, P; Bartels, I; Alsat, EA; Lingen, M; Grzmil, P; Schulze, S; Keyser, J; Weise, D; Borchers, M; Hobbiebrunken, E; Röbl, M; Gärtner, J; Brockmann, K; Zirn, B Journal: Clinical genetics Issue: Volume 83:Number 1(2013:Jan.) Page Start: 53 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Familial occurrence of schwannomas and malignant rhabdoid tumour associated with a duplication in SMARCB1. Issue 1 (5th January 2009) Authors: Swensen, J J; Keyser, J; Coffin, C M; Biegel, J A; Viskochil, D H; Williams, M S Journal: Journal of medical genetics Issue: Volume 46:Issue 1(2009) Page Start: 68 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗