Lee, Hane http://orcid.org/0000-0002-4736-0412
Huang, Alden Y.
Wang, Lee-kai http://orcid.org/0000-0002-7108-2897
Yoon, Amanda J.
Renteria, Genecee
Eskin, Ascia
Signer, Rebecca H.
Dorrani, Naghmeh
Nieves-Rodriguez, Shirley http://orcid.org/0000-0002-2329-4879
Wan, Jijun
Douine, Emilie D.
Woods, Jeremy D. http://orcid.org/0000-0002-3988-9324
Dell’Angelica, Esteban C.
Fogel, Brent L.
Martin, Martin G.
Butte, Manish J. http://orcid.org/0000-0002-4490-5595
Parker, Neil H.
Wang, Richard T.
Shieh, Perry B.
Wong, Derek A.
Gallant, Natalie
Singh, Kathryn E.
Tavyev Asher, Y. Jane
Sinsheimer, Janet S. http://orcid.org/0000-0001-9540-5956
Krakow, Deborah
Loo, Sandra K.
Allard, Patrick
Papp, Jeanette C.
Palmer, Christina
Martinez-Agosto, Julian A.
Nelson, Stanley F. http://orcid.org/0000-0002-2082-3114
Funding for this research was provided by:
National Institutes of Health (T32HG002536)
This article is maintained by: Elsevier
Article Title: Diagnostic utility of transcriptome sequencing for rare Mendelian diseases
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-019-0672-1
Content Type: article
Copyright: © 2020, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics