Additional file 3: Table S2. of Lessons learned from additional research analyses of unsolved clinical exome cases
Year: 2017
Type: dataset
Abstract: De novo and recessive variants in candidate or recently published genes identified by collaboration between BG and BHCMG. (XLSX 28 kb)
Source: Figshare
Authors: Eldomery, Mohammad, Coban-Akdemir, Zeynep, Harel, Tamar, Rosenfeld, Jill, Gambin, Tomasz, AsbjøRg Stray-Pedersen, SÊbastien Kßry, Mercier, Sandra, Lessel, Davor, Denecke, Jonas, Wiszniewski, Wojciech, Penney, Samantha, Pengfei Liu, Weimin Bi, Lalani, Seema, Schaaf, Christian, Wangler, Michael, Bacino, Carlos, Lewis, Richard, Potocki, Lorraine, Graham, Brett, Belmont, John, Scaglia, Fernando, Orange, Jordan, Jhangiani, Shalini, Chiang, Theodore, Harsha Doddapaneni, Jianhong Hu, Muzny, Donna, Xia, Fan, Beaudet, Arthur, Boerwinkle, Eric, Eng, Christine, Plon, Sharon, V. Sutton, Gibbs, Richard, Posey, Jennifer, Yaping Yang, Lupski, James
Language: English
Topic: Genomics and Rare Diseases
Subfield: Genetics
Domain: Life Sciences
Open Access status: green
OpenAlex ID: W4394096640