Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretin...

Por Gehrig, A, Felbor, U, Kelsell, R E, Hunt, D M, Maumenee, I H, Weber, B H
Publicado em 1998

A retGC-1 mutation in autosomal dominant cone-rod dystrophy.

Por Perrault, I, Rozet, J M, Gerber, S, Kelsell, R E, Souied, E, Cabot, A, Hunt, D M, Munnich, A, Kaplan, J
Publicado em 1998

Genetic linkage analysis of a novel syndrome comprising North Carolina-like macular dystrophy and progressive sensorineural hearing loss

Por Francis, P J, Johnson, S, Edmunds, B, Kelsell, R E, Sheridan, E, Garrett, C, Holder, G E, Hunt, D M, Moore, A T
Publicado em 2003

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