Amendola, Laura M.
Berg, Jonathan S.
Horowitz, Carol R.
Angelo, Frank
Bensen, Jeannette T.
Biesecker, Barbara B.
Biesecker, Leslie G.
Cooper, Gregory M.
East, Kelly
Filipski, Kelly
Fullerton, Stephanie M.
Gelb, Bruce D.
Goddard, Katrina A.B.
Hailu, Benyam
Hart, Ragan
Hassmiller-Lich, Kristen
Joseph, Galen
Kenny, Eimear E.
Koenig, Barbara A.
Knight, Sara
Kwok, Pui-Yan
Lewis, Katie L.
McGuire, Amy L.
Norton, Mary E.
Ou, Jeffrey
Parsons, Donald W.
Powell, Bradford C.
Risch, Neil
Robinson, Mimsie
Rini, Christine
Scollon, Sarah
Slavotinek, Anne M.
Veenstra, David L.
Wasserstein, Melissa P.
Wilfond, Benjamin S.
Hindorff, Lucia A.
Plon, Sharon E.
Jarvik, Gail P.
Funding for this research was provided by:
National Human Genome Research Institute (HG200359 09)
This article is maintained by: Elsevier
Article Title: The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations
Journal Title: The American Journal of Human Genetics
CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.ajhg.2018.08.007
Content Type: simple-article
Copyright: © 2018 American Society of Human Genetics.