Additional file 5: Table S3. of A unified analytic framework for prioritization of non-coding variants of uncertain significance in heritable breast and ovarian cancer
Year: 2016
Type: dataset
Abstract: Primer Sequences for Sanger Sequencing of Likely Pathogenic Variants (XLSX 10Â kb)
Source: Figshare
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: green
OpenAlex ID: W4394501296