Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: CATSPER2[original query] |
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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 |
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 |
Homozygous mutations in DZIP1 can induce asthenoteratospermia with severe MMAF. Journal of medical genetics 2020 2 57 (7): 445-453. Lv Mingrong, Liu Wangjie, Chi Wangfei, Ni Xiaoqing, Wang Jiajia, Cheng Huiru, Li Wei-Yu, Yang Shenmin, Wu Huan, Zhang Junqiang, Gao Yang, Liu Chunyu, Li Caihua, Yang Chenyu, Tan Qing, Tang Dongdong, Zhang Jingjing, Song Bing, Chen Yu-Jie, Li Qiang, Zhong Yading, Zhang Zhihua, Saiyin Hexige, Jin Li, Xu Yuping, Zhou Ping, Wei Zhaolian, Zhang Chuanmao, He Xiaojin, Zhang Feng, Cao Yunx |
Pan-Cancer Multiomics Analysis of TC2N Gene Suggests its Important Role(s) in Tumourigenesis of Many Cancers. Asian Pacific journal of cancer prevention : APJCP 2020 11 21 (11): 3199-3209. Qureshi Muhammad Asif, Khan Saeed, Tauheed Muhammad Sohaib, Syed Sofia Ali, Ujjan Ikram Din, Lail Amanullah, Sharafat Shahe |
A simultaneous next-generation sequencing approach to the diagnosis of couple infertility. Minerva endocrinology 2021 5 47 (1): 4-10. Precone Vincenza, Notarangelo Angelantonio, Marceddu Giuseppe, D'Agruma Leonardo, Cannarella Rossella, Calogero Aldo E, Cristofoli Francesca, Guerri Giulia, Paolacci Stefano, Castori Marco, Bertelli Matt |
A whole genome sequencing approach to anterior cruciate ligament rupture-a twin study in two unrelated families. PloS one 2022 10 17 (10): e0274354. Feldmann Daneil, Bope Christian D, Patricios Jon, Chimusa Emile R, Collins Malcolm, September Alison |
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:Apr 16, 2024
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