Entries of Collin, J. Richard O. on the publication server

Ragge, Nicola K., Brown, Alison G., Poloschek, Charlotte M., Lorenz, Birgit, Henderson, R. Alex, Clarke, Michael P., Russell-Eggitt, Isabelle, Fielder, Alistair, Gerrelli, Dianne, Martinez-Barbera, Juan Pedro , Ruddle, Piers, Hurst, Jane, Collin, J. Richard O., Salt, Alison, Cooper, Simon T., Thompson, Pamela J., Sisodiya, Sanjay M., Williamson, Kathleen A., FitzPatrick, David R. , Heyningen, Veronica van and Hanson, Isabel M. (2005) Heterozygous Mutations of OTX2 Cause Severe Ocular Malformations. The American Journal of Human Genetics 76 (6), pp. 1008-1022. Fulltext not available.

Ragge, Nicola K., Lorenz, Birgit, Schneider, Adele, Bushby, Kate, de Sanctis, Luisa, de Sanctis, Ugo, Salt, Alison, Collin, J. Richard O., Vivian, Anthony J., Free, Samantha L., Thompson, Pamela, Williamson, Kathleen A., Sisodiya, Sanjay M., van Heyningen, Veronica and FitzPatrick, David R. (2005) SOX2 anophthalmia syndrome. American Journal of Medical Genetics Part A 135A (1), pp. 1-7. Fulltext not available.