Lincoln, Stephen E.
Hambuch, Tina http://orcid.org/0000-0002-5812-4431
Zook, Justin M.
Bristow, Sara L.
Hatchell, Kathryn
Truty, Rebecca
Kennemer, Michael
Shirts, Brian H.
Fellowes, Andrew
Chowdhury, Shimul
Klee, Eric W.
Mahamdallie, Shazia
Cleveland, Megan H.
Vallone, Peter M.
Ding, Yan
Seal, Sheila
DeSilva, Wasanthi
Tomson, Farol L.
Huang, Catherine
Garlick, Russell K.
Rahman, Nazneen
Salit, Marc
Kingsmore, Stephen F.
Ferber, Matthew J.
Aradhya, Swaroop
Nussbaum, Robert L.
This article is maintained by: Elsevier
Article Title: One in seven pathogenic variants can be challenging to detect by NGS: an analysis of 450,000 patients with implications for clinical sensitivity and genetic test implementation
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-021-01187-w
Content Type: article
Copyright: © 2021, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics