1. Deletions and rearrangements of the H19/IGF2 enhancer region in patients with Silver–Russell syndrome and growth retardation. Issue 5 (28th January 2011) Authors: Grønskov, Karen; Poole, Rebecca L; Hahnemann, Johanne M D; Thomson, Jennifer; Tümer, Zeynep; Brøndum-Nielsen, Karen; Murphy, Rinki; Ravn, Kirstine; Melchior, Linea; Dedic, Alma; Dolmer, Birgitte; Temple, I Karen; Boonen, Susanne E; Mackay, Deborah J G Journal: Journal of medical genetics Issue: Volume 48:Issue 5(2011) Page Start: 308 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes. Issue 4 (5th February 2014) Authors: Docherty, Louise E; Rezwan, Faisal I; Poole, Rebecca L; Jagoe, Hannah; Lake, Hannah; Lockett, Gabrielle A; Arshad, Hasan; Wilson, David I; Holloway, John W; Temple, I Karen; Mackay, Deborah J G Journal: Journal of medical genetics Issue: Volume 51:Issue 4(2014) Page Start: 229 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗