Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Infertility and STRC[original query] |
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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 |
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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- Page last updated:May 06, 2024
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