Chrome Extension
WeChat Mini Program
Use on ChatGLM
VIPCreated with Sketch.

Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study (Genetics in Medicine, (2019), 21, 5, (1100-1110), 10.1038/s41436-018-0308-x)

Ragan Hart,Barbara B. Biesecker,Carrie L. Blout,Kurt D. Christensen,Laura M. Amendola,Katie Bergstrom,Sawona Biswas,Kevin M. Bowling,Laura K. Conlin,Greg M. Cooper,Matthew C. Dulik,Kelly M. East,Jessica Everett,Candice R. Finnila,Arezou A. Ghazani,Marian J. Gilmore,Katrina A.B. Goddard,Gail P. Jarvik,Jennifer J. Johnston,Tia L. Kauffman,Whitley V. Kelley,Joel B. Krier,Katie L. Lewis,Amy L. McGuire,Carmit K. McMullen,Jeffrey Ou,Sharon E. Plon,Heidi L. Rehm,C. Sue Richards,Edward J. Romasko,Ane Miren Sagardia,Nancy B. Spinner,Michelle L. Thompson,Erin Turbitt,Jason L. Vassy,Benjamin S. Wilfond,David L. Veenstra,Jonathan S. Berg,Robert C. Green,Leslie G. Biesecker,Lucia A. Hindorff

Genetics in Medicine（2019）

Cited 4|Views8
No score
Abstract
The originally published version of this Article contained errors in Fig. 2. The numbers below the black arrowheads were incorrect; please see incorrect Figure in associated Correction. These errors have now been corrected in the PDF and HTML versions of the Article.
More
Translated text
Key words
clinical genomic,correction,secondary findings,prevalence,health-care
AI Read Science
Must-Reading Tree
Example
Generate MRT to find the research sequence of this paper
Chat Paper
Summary is being generated by the instructions you defined