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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 - 4 (of 4 Records)

Query Trace: Syndrome and STRC[original query]
Significant Mendelian genetic contribution to pediatric mild-to-moderate hearing loss and its comprehensive diagnostic approach.
Genetics in medicine : official journal of the American College of Medical Genetics 2020 Mar .
Kim Bong Jik, Oh Doo-Yi, Han Jin Hee, Oh Jayoung, Kim Min Young, Park Hye-Rim, Seok Jungirl, Cho Sung-Dong, Lee Sang-Yeon, Kim Yoonjoong, Carandang Marge, Kwon In Sun, Lee Seungmin, Jang Jeong Hun, Choung Yun-Hoon, Lee Sejoon, Lee Hakmin, Hwang Sang Mee, Choi Byung Yo
Prevalence and Characteristics of STRC Gene Mutations (DFNB16): A Systematic Review and Meta-Analysis.
Frontiers in genetics 2021 10 12 707845.
Han Shuang, Zhang Dejun, Guo Yingyuan, Fu Zeming, Guan Guofa
Molecular etiology study of hearing loss in 13 Chinese Han families.
Frontiers in neurology 2022 12 13 1048218.
Sun Lianhua, Lin Zhengyu, Wang Xiaowen, Shen Jiali, Li Yue, Huang Yuyu, Yang J
Frequency of the STRC-CATSPER2 deletion in STRC-associated hearing loss patients.
Scientific reports 2022 1 12 (1): 634.
Nishio Shin-Ya, Usami Shin-Ic
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