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Brain 2019, vol. 142, issue 6
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Genetic Data, Two-Sided Markets and Dynamic Consent: United States Versus France
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A novel nonsense variant in SUPT20H gene associated with Rheumatoid Arthritis identified by Whole Exome Sequencing of multiplex families
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Minor allele of the factor V K858R variant protects from venous thrombosis only in non-carriers of factor V Leiden mutation
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Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F ‐mediated inherited retinal disorders
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OPTIMIR, a novel algorithm for integrating available genome-wide genotype data into miRNA sequence alignment analysis
RNA 2019, vol. 25, issue 6
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