Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Hearing and POU3F4[original query] |
---|
Clinical observations and molecular variables of patients with hearing loss and incomplete partition type III. The Laryngoscope 2015 Nov . Choi Byung Yoon, An Yong-Hwi, Song Jae-Jin, Koo Ja-Won, Lee Jun Ho, Oh Seung Ha, Chang Sun O, Kim Chong Sun, Park Joo Hy |
STRC Deletion is a Frequent Cause of Slight to Moderate Congenital Hearing Impairment in the Czech Republic. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2017 10 38 (10): e393-e400. Plevova Pavlina, Paprskarova Martina, Tvrda Petra, Turska Petra, Slavkovsky Rastislav, Mrazkova E |
Elucidation of the unique mutation spectrum of severe hearing loss in a Vietnamese pediatric population. Scientific reports 2019 Feb 9 (1): 1604. Han Jae Joon, Nguyen Pham Dinh, Oh Doo-Yi, Han Jin Hee, Kim Ah-Reum, Kim Min Young, Park Hye-Rim, Tran Lam Huyen, Dung Nguyen Huu, Koo Ja-Won, Lee Jun Ho, Oh Seung Ha, Anh Vu Hoang, Choi Byung Yo |
First-Line Molecular Genetic Evaluation of Autosomal Recessive Non-Syndromic Hearing Loss. Turkish archives of otorhinolaryngology 2019 10 57 (3): 140-148. Özy?lmaz Berk, Mercan Gül Caner, K?rb?y?k Özgür, Özdemir Taha Re?id, Özkara Samira, Kaya Özge Özer, Kutbay Ya?ar Bekir, Erdo?an Kadri Murat, Güvenç Merve Saka, Koç Alt |
Molecular diagnose of a large hearing loss population from China by targeted genome sequencing. Journal of human genetics 2022 8 67 (11): 643-649. Wu Jie, Cao Zongfu, Su Yu, Wang Yang, Cai Ruikun, Chen Jiyue, Gao Bo, Han Mingyu, Li Xiaohong, Zhang DeJun, Gao Xue, Huang Shasha, Huang Quanfei, Yuan Yongyi, Ma Xu, Dai |
Genetic findings of Sanger and nanopore single-molecule sequencing in patients with X-linked hearing loss and incomplete partition type III. Orphanet journal of rare diseases 2022 2 17 (1): 65. Chen Ying, Qiu Jiajun, Wu Yingwei, Jia Huan, Jiang Yi, Jiang Mengda, Wang Zhili, Sheng Hai-Bin, Hu Lingxiang, Zhang Zhihua, Wang Zhaoyan, Li Yun, Huang Zhiwu, Wu H |
Hereditary etiology of non-syndromic sensorineural hearing loss in the Republic of North Ossetia-Alania. PeerJ 2023 2 11 e14514. Petrova Nika, Tebieva Inna, Kadyshev Vitaly, Getoeva Zalina, Balinova Natalia, Marakhonov Andrey, Vasilyeva Tatyana, Ginter Evgeny, Kutsev Sergey, Zinchenko Re |
- Page last reviewed:Feb 1, 2024
- Page last updated:Mar 25, 2024
- Content source: