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Supplement: mmc3.xlsx › BrM92
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Family-Based Whole-Exome Analysis of Specific Language Impairment (SLI) Identifies Rare Variants in BUD13, a Component of the Retention and Splicing (RES) Complex.
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35053791 (PubMed )
Supplement: brainsci-12-00047-s001.zip › brainsci-1490268_Tables_S1-7_Dec29-2021.xlsx › Table_S5._89var_14q_locus
UV-exposure, endogenous DNA damage, and DNA replication errors shape the spectra of genome changes in human skin.
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Exome and genome sequencing of nasopharynx cancer identifies NF-κB pathway activating mutations.
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Nature Communications, 2017
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A Case of Pulmonary Langerhans Cell Sarcoma Simultaneously Diagnosed with Cutaneous Langerhans Cell Histiocytosis Studied by Whole-Exome Sequencing.
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The impact of tumor profiling approaches and genomic data strategies for cancer precision medicine.
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Genome Medicine, 2016
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Supplement: 13073_2016_333_MOESM4_ESM.xlsx › all_matched_muts.maf
Whole-exome sequencing identifies a recurrent NAB2-STAT6 fusion in solitary fibrous tumors.
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Nature Genetics, 2013
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Supplement: NIHMS474988-supplement-1.pdf
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