Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Deafness and POU3F4[original query] |
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A genome-wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus.
Genes, brain, and behavior 2014 Sep 13 (7): 675-85. Cai D-C, Fonteijn H, Guadalupe T, Zwiers M, Wittfeld K, Teumer A, Hoogman M, Arias-Vásquez A, Yang Y, Buitelaar J, Fernández G, Brunner H G, van Bokhoven H, Franke B, Hegenscheid K, Homuth G, Fisher S E, Grabe H J, Francks C, Hagoort |
Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations. BMC medical genetics 2015 16 9. Bademci Guney, Lasisi Akeem, Yariz Kemal O, Montenegro Paola, Menendez Ibis, Vinueza Rodrigo, Paredes Rosario, Moreta Germania, Subasioglu Asli, Blanton Susan, Fitoz Suat, Incesulu Armagan, Sennaroglu Levent, Tekin Musta |
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 |
Next-Generation Sequencing Identifies Pathogenic Variants in HGF, POU3F4, TECTA, and MYO7A in Consanguineous Pakistani Deaf Families. Neural plasticity 2021 5 2021 5528434. Mei Xueshuang, Zhou Yaqi, Amjad Muhammad, Yang Weiqiang, Zhu Rufei, Asif Muhammad, Hussain Hafiz Muhammad Jafar, Yang Tao, Iqbal Furhan, Hu Hong |
Study of complex structural variations of X-linked deafness-2 based on single-molecule sequencing. Bioscience reports 2021 Apr . Jiang Yi, Wu Lihua, Huang Shasha, Li Pidong, Gao Bo, Yuan Yongyi, Zhang Siwen, Yu Guoliang, Gao Yong, Wu Hao, 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 |
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