Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Hearing Loss and F2[original query] |
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Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation. Mitochondrion 2010 Jan 10 (1): 69-81. Lu Jianxin, Qian Yaping, Li Zhiyuan, Yang Aifen, Zhu Yi, Li Ronghua, Yang Li, Tang Xiaowen, Chen Bobei, Ding Yu, Li Yongyan, You Junyan, Zheng Jing, Tao Zhihua, Zhao Fuxin, Wang Jindan, Sun Dongmei, Zhao Jianyue, Meng Yanzi, Guan Min-X |
The genes for sensory perception of sound should be considered in gene diagnosis of congenital sensorineural hearing loss and microtia. Journal of applied genetics 2022 1 63 (2): 327-337. Lin Ken, You Ding-Yun, Zhang Li-Huan, Zhou Li-Juan, Zu Jin-Yan, Xiao Yang, Sun Mei-Hua, Dong-Su , Cao Xue, Zhang Tie-Song, Ma Ji |
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