A genetic linkage study of a kindred with X-linked retinitis pigmentosa.

Por Bhattacharya, S S, Clayton, J F, Harper, P S, Hoare, G W, Jay, M R, Lyness, A L, Wright, A F
Publicado em 1985

Further refinement of the location for autosomal dominant retinitis pigmentosa on chromosome 7p (RP9).

Por Inglehearn, C. F., Keen, T. J., al-Maghtheh, M., Gregory, C. Y., Jay, M. R., Moore, A. T., Bird, A. C., Bhattacharya, S. S.
Publicado em 1994

Ocular findings associated with a 3 base pair deletion in the peripherin-RDS gene in autosomal dominant retinitis pigmentosa.

Por Wroblewski, J J, Wells, J A, Eckstein, A, Fitzke, F W, Jubb, C, Keen, T J, Inglehearn, C F, Bhattacharya, S S, Arden, G B, Jay, M R
Publicado em 1994

Localization of a gene (CORD7) for a dominant cone-rod dystrophy to chromosome 6q.

Por Kelsell, R E, Gregory-Evans, K, Gregory-Evans, C Y, Holder, G E, Jay, M R, Weber, B H, Moore, A T, Bird, A C, Hunt, D M
Publicado em 1998