Updates are available Correction dated 2019-01-22
Click to view Correction: https://doi.org/10.1038/s41436-019-0440-2
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Authors
Hart, M. Ragan
Biesecker, Barbara B.
Blout, Carrie L.
Christensen, Kurt D.
Amendola, Laura M.
Bergstrom, Katie L.
Biswas, Sawona
Bowling, Kevin M.
Brothers, Kyle B.
Conlin, Laura K.
Cooper, Greg M.
Dulik, Matthew C.
East, Kelly M.
Everett, Jessica N.
Finnila, Candice R.
Ghazani, Arezou A.
Gilmore, Marian J.
Goddard, Katrina A. B
Jarvik, Gail P.
Johnston, Jennifer J.
Kauffman, Tia L.
Kelley, Whitley V.
Krier, Joel B.
Lewis, Katie L.
McGuire, Amy L.
McMullen, Carmit
Ou, Jeffrey
Plon, Sharon E.
Rehm, Heidi L.
Richards, C. Sue
Romasko, Edward J.
Miren Sagardia, Ane
Spinner, Nancy B.
Thompson, Michelle L.
Turbitt, Erin
Vassy, Jason L.
Wilfond, Benjamin S.
Veenstra, David L.
Berg, Jonathan S.
Green, Robert C.
Biesecker, Leslie G.
Hindorff, Lucia A.
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More Information
This article is maintained by: Elsevier
Article Title: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-018-0308-x
Content Type: article
Copyright: © 2019, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics
