Using high-resolution variant frequencies to empower clinical genome interpretation
Autor: | Whiffin, Nicola, Minikel, Eric, Walsh, Roddy, O’Donnell-Luria, Anne H, Karczewski, Konrad, Ing, Alexander Y, Barton, Paul J R, Funke, Birgit, Cook, Stuart A, MacArthur, Daniel, Ware, James S |
---|---|
Zdroj: | In Genetics in Medicine October 2017 19(10):1151-1158 |
Databáze: | ScienceDirect |
Externí odkaz: |