Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: CEP63[original query] |
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Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family. Human genetics 2015 Sep . Einarsdottir Elisabet, Svensson Idor, Darki Fahimeh, Peyrard-Janvid Myriam, Lindvall Jessica M, Ameur Adam, Jacobsson Christer, Klingberg Torkel, Kere Juha, Matsson Ha |
Copy Number Variations of CEP63, FOSL2 and PAQR6 Serve as Novel Signatures for the Prognosis of Bladder Cancer. Frontiers in oncology 2021 11 674933. Cai Zhao, Chen Huang, Bai Jingqiao, Zheng Yang, Ma Jianhui, Cai Xiongwei, Liu Yu, Zhang Kaitai, Shou Jianzhong, Gao Yanni |
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- |
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