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

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Dades bibliogràfiques
Publicat a:Am J Hum Genet
Autors principals: 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
Idioma:Inglês
Publicat: Elsevier 2019
Matèries:
Letters to the Editor
Accés en línia: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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