Assessing the correlation between mutant rhodopsin stability and the severity of retinitis pigmentosa

by McKeone, Richard, Wikstrom, Matthew, Kiel, Christina, Rakoczy, P. Elizabeth
Published 2014

Foxf2: A Novel Locus for Anterior Segment Dysgenesis Adjacent to the Foxc1 Gene

by McKeone, Richard, Vieira, Helena, Gregory-Evans, Kevin, Gregory-Evans, Cheryl Y., Denny, Paul
Published 2011

Organization and Evolution of a Gene-Rich Region of the Mouse Genome: A 12.7-Mb Region Deleted in the Del(13)Svea36H Mouse

by Mallon, Ann-Marie, Wilming, Laurens, Weekes, Joseph, Gilbert, James G.R., Ashurst, Jennifer, Peyrefitte, Sandrine, Matthews, Lucy, Cadman, Matthew, McKeone, Richard, Sellick, Chris A., Arkell, Ruth, Botcherby, Marc R.M., Strivens, Mark A., Campbell, R. Duncan, Gregory, Simon, Denny, Paul, Hancock, John M., Rogers, Jane, Brown, Steve D.M.
Published 2004

Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen

by Bogani, Debora, Willoughby, Catherine, Davies, Jennifer, Kaur, Kulvinder, Mirza, Ghazala, Paudyal, Anju, Haines, Heather, McKeone, Richard, Cadman, Matthew, Pieles, Guido, Schneider, Jürgen E., Bhattacharya, Shoumo, Hardy, Andrea, Nolan, Patrick M., Tripodis, Nikos, Depew, Michael J., Chandrasekara, Ramya, Duncan, Gimara, Sharpe, Paul T., Greenfield, Andy, Denny, Paul, Brown, Steve D. M., Ragoussis, Jiannis, Arkell, Ruth M.
Published 2005