Medicine and Dentistry
Diseases
100%
Phenotype
63%
Retina Degeneration
63%
Photoreceptor
54%
Development
36%
Gene
36%
Therapeutic Procedure
36%
Retina
36%
Combination Therapy
27%
Family
27%
Comprehension
27%
Patient
27%
Genetic Disorder
18%
Pathogenesis
18%
Genetic Heterogeneity
18%
Autosomal Dominant Inheritance
18%
Visual Impairment
18%
Next Generation Sequencing
18%
Familial Exudative Vitreoretinopathy
18%
Death
18%
Prognosis
18%
Clinical Trial
18%
Amaurosis
18%
Genetic Screening
9%
Diagnosis
9%
Vascularity
9%
Vision
9%
Autosomal Recessive Inheritance
9%
Visual Acuity
9%
Genotype Phenotype Correlation
9%
Retinitis pigmentosa
9%
Optical Coherence Tomography
9%
Therapeutic Window
9%
Dystrophy
9%
Angioid Streak
9%
Stargardt Disease
9%
Assessment
9%
Biochemistry, Genetics and Molecular Biology
Phenotype
63%
Development
36%
Genetics
36%
Nested Gene
27%
Vision
27%
Comprehension
27%
Autosomal Dominant Inheritance
18%
Genetic Heterogeneity
18%
Genetic Disorder
18%
Quantitative Technique
9%
Optics
9%
Autosomal Recessive Inheritance
9%
Vascularization
9%
Visual Acuity
9%
Retinitis pigmentosa
9%
Genotype Phenotype Correlation
9%
Genetic Screening
9%
Genome Editing
9%
Neuroscience
Phenotype
63%
Retinal Degeneration
63%
Gene
27%
Retinitis pigmentosa
9%
Angioid Streak
9%