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Genome Research|February 1, 1996
Sorsby's fundus dystrophy in the British Isles: demonstration of a striking founder effect by microsatellite-generated haplotypesS D Wijesuriya, K Evans, M R Jay, et al.
Human Genetics|September 10, 1999
Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locusI Zito, D L Thiselton, M B Gorin, et al.
The British Journal of Ophthalmology|August 1, 1993
Autosomal dominant retinitis pigmentosa with apparent incomplete penetrance: a clinical, electrophysiological, psychophysical, and molecular genetic studyA T Moore, F Fitzke, M Jay, et al.
Human Molecular Genetics|February 1, 1994
Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19M al-Maghtheh, C F Inglehearn, T J Keen, et al.
The British Journal of Ophthalmology|January 1, 1995
Autosomal dominant retinitis pigmentosa mapping to chromosome 7p exhibits variable expressionR Y Kim, F W Fitzke, A T Moore, et al.
The American Journal of Pathology|August 12, 2014
Mutations in pre-mRNA processing factors 3, 8, and 31 cause dysfunction of the retinal pigment epitheliumMichael H Farkas, Deborah S Lew, Maria E Sousa, et al.
Clinical and Experimental Obstetrics & Gynecology|March 15, 2003
Can human fetal cortical brain tissue transplant (up to 20 weeks) sustain its metabolic and oxygen requirements in a heterotopic site outside the brain? A study of 12 volunteers with Parkinson's diseaseN Bhattacharya, M K Chhetri, K L Mukherjee, et al.
Journal of Experimental & Clinical Cancer Research : CR|October 19, 2002
Antineoplastic effect of new boron compounds against leukemic cell lines and cells from leukemic patientsN Murmu, P Ghosh, A Gomes, et al.
Human Genetics|October 1, 1986
Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 (L1.28): further linkage data, heterogeneity testing, and risk estimationJ F Clayton, A F Wright, M Jay, et al.
Genomics|April 12, 2002
An integrated, functionally annotated gene map of the DXS8026-ELK1 interval on human Xp11.3-Xp11.23: potential hotspot for neurogenetic disordersDawn L Thiselton, Jennifer McDowall, Oliver Brandau, et al.
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