Loci for autosomal dominant retinitis pigmentosa and dominant cystoid macular dystrophy on chromosome 7p are not allelic.

von Inglehearn, C., Keen, T. J., al-Maghtheh, M., Bhattacharya, S.
Veröffentlicht 1994

RP11 is the second most common locus for dominant retinitis pigmentosa.

von Vithana, E, Al-Maghtheh, M, Bhattacharya, S S, Inglehearn, C F
Veröffentlicht 1998

Simple tests for rhodopsin involvement in retinitis pigmentosa.

von Tarttelin, E, Al-Maghtheh, M, Keen, J, Bhattacharya, S, Inglehearn, C
Veröffentlicht 1996

Segregation of a PRKCG mutation in two RP11 families.

von Al-Maghtheh, M, Vithana, E N, Inglehearn, C F, Moore, T, Bird, A C, Bhattacharya, S S
Veröffentlicht 1998

Evidence for a major retinitis pigmentosa locus on 19q13.4 (RP11) and association with a unique bimodal expressivity phenotype.

von Al-Maghtheh, M., Vithana, E., Tarttelin, E., Jay, M., Evans, K., Moore, T., Bhattacharya, S., Inglehearn, C. F.
Veröffentlicht 1996

A linkage survey of 20 dominant retinitis pigmentosa families: frequencies of the nine known loci and evidence for further heterogeneity.

von Inglehearn, C F, Tarttelin, E E, Plant, C, Peacock, R E, al-Maghtheh, M, Vithana, E, Bird, A C, Bhattacharya, S S
Veröffentlicht 1998

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

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

Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19q.

von Evans, K, al-Maghtheh, M, Fitzke, F W, Moore, A T, Jay, M, Inglehearn, C F, Arden, G B, Bird, A C
Veröffentlicht 1995