Using High-Resolution Variant Frequencies Empowers Clinical Genome Interpretation and Enables Investigation of Genetic Architecture

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Bibliografski detalji
Izdano u:Am J Hum Genet
Glavni autori: Whiffin, Nicola, Roberts, Angharad M., Minikel, Eric, Zappala, Zach, Walsh, Roddy, O’Donnell-Luria, Anne H., Karczewski, Konrad J., Harrison, Steven M., Thomson, Kate L., Sage, Helen, Ing, Alexander Y., Barton, Paul J.R., Funke, Birgit, Cook, Stuart A., MacArthur, Daniel G., Ware, James S.
Format: Artigo
Jezik:Inglês
Izdano: Elsevier 2019
Teme:
Letters to the Editor
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6323549/
https://ncbi.nlm.nih.gov/pubmed/30609406
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2018.11.012
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