Detection and impact of rare regulatory variants in human disease.
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A community-based resource for automatic exome variant-calling and annotation in Mendelian disorders.Non-Coding Loss-of-Function Variation in Human Genomes.SuRFing the genomics wave: an R package for prioritising SNPs by functionalityAn integrative computational approach for prioritization of genomic variantsThe impact of structural variation on human gene expression.Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk.
P2860
Detection and impact of rare regulatory variants in human disease.
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article científic
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article scientifique
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Detection and impact of rare regulatory variants in human disease.
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Detection and impact of rare regulatory variants in human disease.
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Detection and impact of rare regulatory variants in human disease.
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P2860
P356
P1476
Detection and impact of rare regulatory variants in human disease.
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P2093
Stephen B Montgomery
P2860
P356
10.3389/FGENE.2013.00067
P577
2013-05-31T00:00:00Z