Human Genome Epidemiology Literature Finder
Records 1 - 1 (of 1 Records) |
Query Trace: Deafness and SALL1[original query] |
---|
Next-generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss. Molecular genetics & genomic medicine 2020 Oct e1539. Xiang Yan-Bao, Xu Chen-Yang, Xu Yun-Zhi, Li Huan-Zheng, Zhou Li-Li, Xu Xue-Qin, Chen Zi-Hui, Tang Shao-H |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: