Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: RFT1[original query] |
---|
Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants.
HGG advances 2022 12 4 (1): 100163. Young Kristin L, Fisher Virginia, Deng Xuan, Brody Jennifer A, Graff Misa, Lim Elise, Lin Bridget M, Xu Hanfei, Amin Najaf, An Ping, Aslibekyan Stella, Fohner Alison E, Hidalgo Bertha, Lenzini Petra, Kraaij Robert, Medina-Gomez Carolina, Proki? Ivana, Rivadeneira Fernando, Sitlani Colleen, Tao Ran, van Rooij Jeroen, Zhang Di, Broome Jai G, Buth Erin J, Heavner Benjamin D, Jain Deepti, Smith Albert V, Barnes Kathleen, Boorgula Meher Preethi, Chavan Sameer, Darbar Dawood, De Andrade Mariza, Guo Xiuqing, Haessler Jeffrey, Irvin Marguerite R, Kalyani Rita R, Kardia Sharon L R, Kooperberg Charles, Kim Wonji, Mathias Rasika A, McDonald Merry-Lynn, Mitchell Braxton D, Peyser Patricia A, Regan Elizabeth A, Redline Susan, Reiner Alexander P, Rich Stephen S, Rotter Jerome I, Smith Jennifer A, Weiss Scott, Wiggins Kerri L, Yanek Lisa R, Arnett Donna, Heard-Costa Nancy L, Leal Suzanne, Lin Danyu, McKnight Barbara, Province Michael, van Duijn Cornelia M, North Kari E, Cupples L Adrienne, Liu Ching- |
The mutational profile in a South African cohort with inherited neuropathies and spastic paraplegia. Frontiers in neurology 2023 9 14 1239725. Amokelani C Mahungu, Elizabeth Steyn, Niki Floudiotis, Lindsay A Wilson, Jana Vandrovcova, Mary M Reilly, Christopher J Record, Michael Benatar, Gang Wu, Sharika Raga, Jo M Wilmshurst, Kireshnee Naidu, Michael Hanna, Melissa Nel, Jeannine M Heckma |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: