1. Targeted long-read sequencing identifies missing disease-causing variation
- Author
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Miller, Danny E., primary, Sulovari, Arvis, additional, Wang, Tianyun, additional, Loucks, Hailey, additional, Hoekzema, Kendra, additional, Munson, Katherine M., additional, Lewis, Alexandra P., additional, Fuerte, Edith P. Almanza, additional, Paschal, Catherine R., additional, Walsh, Tom, additional, Thies, Jenny, additional, Bennett, James T., additional, Glass, Ian, additional, Dipple, Katrina M., additional, Patterson, Karynne, additional, Bonkowski, Emily S., additional, Nelson, Zoe, additional, Squire, Audrey, additional, Sikes, Megan, additional, Beckman, Erika, additional, Bennett, Robin L., additional, Earl, Dawn, additional, Lee, Winston, additional, Allikmets, Rando, additional, Perlman, Seth J., additional, Chow, Penny, additional, Hing, Anne V., additional, Wenger, Tara L., additional, Adam, Margaret P., additional, Sun, Angela, additional, Lam, Christina, additional, Chang, Irene, additional, Zou, Xue, additional, Austin, Stephanie L., additional, Huggins, Erin, additional, Safi, Alexias, additional, Iyengar, Apoorva K., additional, Reddy, Timothy E., additional, Majoros, William H., additional, Allen, Andrew S., additional, Crawford, Gregory E., additional, Kishnani, Priya S., additional, King, Mary-Claire, additional, Cherry, Tim, additional, Chong, Jessica X., additional, Bamshad, Michael J., additional, Nickerson, Deborah A., additional, Mefford, Heather C., additional, Doherty, Dan, additional, and Eichler, Evan E., additional
- Published
- 2021
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