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Publications by G.Jane Farrar
Autosomal Dominant Retinitis Pigmentosa: A New Multi-Allelic Marker (D3S621) Genetically Linked to the Disease Locus (RP4)
Human Genetics
Genetics
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Bimodal Expressivity in Dominant Retinitis Pigmentosa Genetically Linked to Chromosome 19q.
British Journal of Ophthalmology
Molecular Neuroscience
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Presence of a Triple Concentric Autofluorescence Ring inNR2E3-p.G56R–Linked Autosomal Dominant Retinitis Pigmentosa (ADRP)
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
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Linkage Analysis of Five Pedigrees Affected With Typical Autosomal Dominant Retinitis Pigmentosa.
Journal of Medical Genetics
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Genomic Rearrangements of thePRPF31Gene Account for 2.5% of Autosomal Dominant Retinitis Pigmentosa
Investigative Ophthalmology and Visual Science
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Phenotype-Genotype Correlations in Autosomal Dominant Retinitis Pigmentosa Caused by RHO, D190N
Current Eye Research
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Ophthalmology
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A New Locus for Autosomal Dominant Stargardt-Like Disease Maps to Chromosome 4
American Journal of Human Genetics
Genetics
Mapping the RP10 Locus for Autosomal Dominant Retinitis Pigmentosa on 7q: Refined Genetic Positioning and Localization Within a Well-Defined YAC Contig.
Genome Research
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Mutations in Known Genes Account for 58% of Autosomal Dominant Retinitis Pigmentosa (adRP)
Advances in Experimental Medicine and Biology
Biochemistry
Medicine
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Molecular Biology
Abnormal Dark Adaptation Kinetics in Autosomal Dominant Sector Retinitis Pigmentosa Due to Rod Opsin Mutation.
British Journal of Ophthalmology
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