Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 4 (of 4 Records)

Query Trace: Deafness and COL11A1[original query]
Target sequencing of 307 deafness genes identifies candidate genes implicated in microtia.
Oncotarget 2017 Sep 8 (38): 63324-63332.
Wang Pu, Fan Xinmiao, Wang Yibei, Fan Yue, Liu Yaping, Zhang Shuyang, Chen Xiaow
Splice-altering variant in COL11A1 as a cause of nonsyndromic hearing loss DFNA37.
Genetics in medicine : official journal of the American College of Medical Genetics 2018 9 21 (4): 948-954.
Booth Kevin T, Askew James W, Talebizadeh Zohreh, Huygen Patrick L M, Eudy James, Kenyon Judith, Hoover Denise, Hildebrand Michael S, Smith Katherine R, Bahlo Melanie, Kimberling William J, Smith Richard J H, Azaiez Hela, Smith Shelley
Multi-Center in-Depth Screening of Neonatal Deafness Genes: Zhejiang, China.
Frontiers in genetics 2021 12 637096.
Cai Luhang, Liu Ya, Xu Yaping, Yang Hang, Lv Lihui, Li Yang, Chen Qiongqiong, Lin Xiaojiang, Yang Yihui, Hu Guangwei, Zheng Guofeng, Zhou Jing, Qian Qiyong, Xu Mei-Ai, Fang Jin, Ding Jianjun, Chen Wei, Gao Jio
Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria.
European journal of human genetics : EJHG 2021 Nov .
Adeyemo Adebolajo, Faridi Rabia, Chattaraj Parna, Yousaf Rizwan, Tona Risa, Okorie Samuel, Bharadwaj Thashi, Nouel-Saied Liz M, Acharya Anushree, Schrauwen Isabelle, Morell Robert J, Leal Suzanne M, Friedman Thomas B, Griffith Andrew J, Roux Isabel
TOP