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Now showing items 1-5 of 5
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
An analysis of tissue-specific alternative splicing at the protein level.
Analysis of the immune microenvironment in resected non-small cell lung cancer: the prognostic value of different T lymphocyte markers.
Disruption of NIPBL/Scc2 in Cornelia de Lange Syndrome provokes cohesin genome-wide redistribution with an impact in the transcriptome.
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer