Catherine Plant

Linkage of congenital hereditary endothelial dystrophy to chromosome 20

Naoki Toma, Neil D. Ebenezer, Chris F. Inglehearn et al. · Human Molecular Genetics · 1995 · 135 citations

Life Sciences, Genetics, Molecular Genetics +9

Intrafamilial variation of phenotype in Stargardt macular dystrophy-Fundus flavimaculatus.

Noemi Lois, Graham E. Holder, F.W. Fitzke et al. · PubMed · 1999 · 103 citations

Medicine, Genetics, Ophthalmology +17

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

Rosemary E. Kelsell, Bernard F. Godley, Kevin Gregory-Evans et al. · Human Molecular Genetics · 1995 · 65 citations

Life Sciences, Genetics, Ophthalmology +15

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

Chris F. Inglehearn, Emma E. Tarttelin, Catherine Plant et al. · Journal of Medical Genetics · 1998 · 53 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locus

Ilaria Zito, Dawn L. Thiselton, Michael B. Gorin et al. · Human Genetics · 1999 · 42 citations

Medicine, Genetics, Molecular Genetics +6