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Publications by S P Daiger
Mapping the RP10 Locus for Autosomal Dominant Retinitis Pigmentosa on 7q: Refined Genetic Positioning and Localization Within a Well-Defined YAC Contig.
Genome Research
Genetics
Related publications
Autosomal Dominant Retinitis Pigmentosa: A New Multi-Allelic Marker (D3S621) Genetically Linked to the Disease Locus (RP4)
Human Genetics
Genetics
Genomic Rearrangements of thePRPF31Gene Account for 2.5% of Autosomal Dominant Retinitis Pigmentosa
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Genetic and Physical Mapping of the Locus for Autosomal Dominant Renal Fanconi Syndrome, on Chromosome 15q15.3
American Journal of Human Genetics
Genetics
Mutations in Known Genes Account for 58% of Autosomal Dominant Retinitis Pigmentosa (adRP)
Advances in Experimental Medicine and Biology
Biochemistry
Medicine
Genetics
Molecular Biology
Linkage Analysis of Five Pedigrees Affected With Typical Autosomal Dominant Retinitis Pigmentosa.
Journal of Medical Genetics
Genetics
Phenotype-Genotype Correlations in Autosomal Dominant Retinitis Pigmentosa Caused by RHO, D190N
Current Eye Research
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Long-Range Mapping and Construction of a YAC Contig Within the Cat Eye Syndrome Critical Region.
Genome Research
Genetics
A Rhodopsin Gene Mutation Responsible for Autosomal Dominant Retinitis Pigmentosa Results in a Protein That Is Defective in Localization to the Photoreceptor Outer Segment
Journal of Neuroscience
Neuroscience
Presence of a Triple Concentric Autofluorescence Ring inNR2E3-p.G56R–Linked Autosomal Dominant Retinitis Pigmentosa (ADRP)
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
