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American Journal of Medical Genetics. Part A|June 17, 2015
Targeted gene capture and massively parallel sequencing identify TMC1 as the causative gene in a six-generation Chinese family with autosomal dominant hearing lossXue Gao, Sha-Sha Huang, Yong-Yi Yuan, et al.Genetic Testing and Molecular Biomarkers|July 29, 2010
Analysis of a large-scale screening of mitochondrial DNA m.1555A>G mutation in 2417 deaf-mute students in northwest of ChinaYu-Fen Guo, Xiao-Wen Liu, Bai-Cheng Xu, et al.International Journal of Pediatric Otorhinolaryngology|May 21, 2010
Identification of two novel mutations, c.232T>C and c.2006A>T, in SLC26A4 in a Chinese family associated with enlarged vestibular aqueductYu-Fen Guo, Yan-Li Wang, Bai-Cheng Xu, et al.Biochimica Et Biophysica Acta. Molecular Basis of Disease|August 18, 2020
KLF2 regulates neutrophil migration by modulating CXCR1 and CXCR2 in asthmaLi-Ming Zhu, Dan Zeng, Xue-Chun Lei, et al.BMC Medical Genetics|May 28, 2010
Screening mutations of OTOF gene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathyDa-Yong Wang, Yi-Chen Wang, Dominique Weil, et al.Pageof 7