Evaluation of array CGH platforms for clinical diagnostic purposes using idiopathic learning disability as a model condition. by Regan, R, Smith, K, Crocker, M, Guiver, C, Taylor, J, Knight, S

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome. by Sharp, A, Hansen, S, Selzer, R, Cheng, Z, Regan, R, Hurst, J, Stewart, H, Price, S, Blair, E, Hennekam, R, Fitzpatrick, C, Segraves, R, Richmond, T, Guiver, C, Albertson, D, Pinkel, D, Eis, P, Schwartz, S, Knight, S, Eichler, E