D. Hunt

A human homolog of yeast pre-mRNA splicing gene, PRP31, underlies autosomal dominant retinitis pigmentosa on chromosome 19q13.4 (RP11).

D. Hunt, A. Bird, S. Bhattacharya, 2001, Molecular cell.

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

D. Hunt, A. Bird, M. Jay, 1998, American journal of human genetics.

Blue cone monochromatism: a phenotype and genotype assessment with evidence of progressive loss of cone function in older individuals

J. Mollon, D. Hunt, G. Holder, 2005, Eye.

Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6q.

A. Bird, A. Moore, C. Gregory, 1995, Human molecular genetics.

Linkage investigation of three putative tuberous sclerosis determining loci on chromosomes 9q, llq, and 12q

M. Pericak-Vance, Cardiff, S. Povey, 2022 .

North Carolina macular dystrophy (MCDR1) locus: a fine resolution genetic map and haplotype analysis.

M. Pericak-Vance, C. Flaxel, D. Saperstein, 1999, Molecular vision.