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Diseases2

Retinal Dystrophies Genetic Diseases, Inborn

Analytical, Diagnostic and Therapeutic Techniques and Equipment3

Sequence Analysis, DNA High-Throughput Nucleotide Sequencing Pedigree

Phenomena and Processes8

Exome Genome, Human Mutation Mutation, Missense Exons Polymorphism, Single Nucleotide DNA Copy Number Variations Homozygote

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