HuGE Literature Finder
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Mutational spectrum and clinical features of patients with ACTG1 mutations identified by massively parallel DNA sequencing. The Annals of otology, rhinology, and laryngology 2015 May 124 Suppl 1 84S-93S. Miyagawa Maiko, Nishio Shin-Ya, Ichinose Aya, Iwasaki Satoshi, Murata Takaaki, Kitajiri Shin-Ichiro, Usami Shin-Ic |
Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss. Journal of translational medicine 2014 12 (1): 311. Wei Qinjun, Zhu Hongmei, Qian Xuli, Chen Zhibin, Yao Jun, Lu Yajie, Cao Xin, Xing Guangqi |
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