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Publications by Patricia Forsythe
Analysis of the RPGRGene in 11 Pedigrees With the Retinitis Pigmentosa Type 3 Genotype: Paucity of Mutations in the Coding Region but Splice Defects in Two Families
American Journal of Human Genetics
Genetics
Related publications
Association of Pathogenic Mutations in TULP1 With Retinitis Pigmentosa in Consanguineous Pakistani Families
Archives of Ophthalmology
Linkage Analysis of Five Pedigrees Affected With Typical Autosomal Dominant Retinitis Pigmentosa.
Journal of Medical Genetics
Genetics
Rhodopsin Mutations in Chinese Patients With Retinitis Pigmentosa
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Phenotype-Genotype Correlations in X Linked Retinitis Pigmentosa.
Journal of Medical Genetics
Genetics
Prp8 Retinitis Pigmentosa Mutants Cause Defects in the Transition Between the Catalytic Steps of Splicing
RNA
Molecular Biology
Advances in the Understanding of Retinitis Pigmentosa
Eye
Medicine
Arts
Sensory Systems
Ophthalmology
Humanities
Mutation Analysis of the RPGR Gene Reveals Novel Mutations in South European Patients With X-Linked Retinitis Pigmentosa
European Journal of Human Genetics
Genetics
Tau Pathology in Two Dutch Families With Mutations in the Microtubule-Binding Region of Tau
American Journal of Pathology
Forensic Medicine
Pathology
High Prevalence of Mutations in theEYSGene in Japanese Patients With Autosomal Recessive Retinitis Pigmentosa
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
