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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Hearing Loss and TRIOBP[original query]
Genetic testing for sporadic hearing loss using targeted massively parallel sequencing identifies 10 novel mutations.
Clinical genetics 2015 Jun 87 (6): 588-93.
Gu X, Guo L, Ji H, Sun S, Chai R, Wang L, Li
A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records. GWAS Catalog
PLoS genetics 2016 Oct 12 (10): e1006371.
Hoffmann Thomas J, Keats Bronya J, Yoshikawa Noriko, Schaefer Catherine, Risch Neil, Lustig Lawrence
Targeted Next-Generation Sequencing of a Deafness Gene Panel (MiamiOtoGenes) Analysis in Families Unsuitable for Linkage Analysis.
BioMed research international 2018 3 2018 3103986.
Shang Haiqiong, Yan Denise, Tayebi Naeimeh, Saeidi Kolsoum, Sahebalzamani Afsaneh, Feng Yong, Blanton Susan, Liu Xuezho
Whole-exome sequencing identifies rare pathogenic and candidate variants in sporadic Chinese Han deaf patients.
Clinical genetics 2019 9 97 (2): 352-356.
Zou Songfeng, Mei Xueshuang, Yang Weiqiang, Zhu Rvfei, Yang Tao, Hu Hong
Case Report: Novel Compound Heterozygous Variants in TRIOBP Associated With Congenital Deafness in a Chinese Family.
Frontiers in genetics 2021 12 12 766973.
Zhou Cong, Xiao Yuanyuan, Xie Hanbing, Wang Jing, Liu Shanli
Analysis of TRIOBP gene in non-syndromic deafness: A case report.
Medicine 2024 11 103 (45): e40435.
Hong Zhou, Gang Guo, Jianjun Gao, Hong Du
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