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Gonzalez Juan R. The identification of these latter two unknown metabolites as medium-chain length acylcarnitines is coherent with reports by Adams et al. Turley Patrick ; M. Finally, M, MT and AV.

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Elyanow, rebecca; wu, hsin-ta; raphael, benjamin j structural variation, including large deletions, duplications, inversions, translocations, and other rearrangements, is common in human and cancer genomes.

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This is often achieved by comparing nonsynonymous variants between unrelated patients, and particularly for sporadic or recessive disease, often identifies a single or few candidate genes for further consideration. posts tagged ‘genome-wide association study’

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Jadwiga ; A. Here we highlight the potential for exome sequencing to identify a reasonable of candidate genes when dominant disease variants are inherited from a mosaic parent.

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The and type of the metabolic features that went into these GWAS was mainly defined by the metabolomics techniques used: Gieger et al. These barcoded re contain long-range sequence information that is advantageous for identification of structural variants. Dalton C?

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