Human microphthalmia associated with mutations in the retinal homeobox gene CHX10. - Ferda Percin, E.; Ploder, Lynda A.; Yu, Jessica J.; Arici, Kemal; Jonathan Horsford, D.; Rutherford, Adam; Bapat, Bharati; Cox, Diane W.; Duncan, Alessandra M.V.; Kalnins, Vitauts I.; Kocak-Altintas, Aysegul; Sowden, Jane C.; et al. (Nature Genetics, 2000)