Evolution of the Alx homeobox gene family: parallel retention and independent loss of the vertebrate Alx3 gene. by McGonnell, I, Graham, A, Richardson, J, Fish, J, Depew, M, Dee, C, Holland, P, Takahashi, T

Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen. by Bogani, D, Willoughby, C, Davies, J, Kaur, K, Mirza, G, Paudyal, A, Haines, H, McKeone, R, Cadman, M, Pieles, G, Schneider, J, Bhattacharya, S, Hardy, A, Nolan, P, Tripodis, N, Depew, M, Chandrasekara, R, Duncan, G, Sharpe, P, Greenfield, A, Denny, P, Brown, S, Ragoussis, J, Arkell, R