Item request has been placed!
×
Item request cannot be made.
×
Processing Request
Genetic findings of Sanger and nanopore single-molecule sequencing in patients with X-linked hearing loss and incomplete partition type III.
Item request has been placed!
×
Item request cannot be made.
×
Processing Request
- المؤلفون: Chen, Ying1,2,3 (AUTHOR); Qiu, Jiajun1,2,3 (AUTHOR); Wu, Yingwei4 (AUTHOR); Jia, Huan1,2,3 (AUTHOR); Jiang, Yi1,2,3 (AUTHOR); Jiang, Mengda4 (AUTHOR); Wang, Zhili1,2,3 (AUTHOR); Sheng, Hai-Bin1,2,3 (AUTHOR); Hu, Lingxiang1,2,3 (AUTHOR); Zhang, Zhihua1,2,3 (AUTHOR); Wang, Zhaoyan1,2,3 (AUTHOR); Li, Yun1,2,3 (AUTHOR) ; Huang, Zhiwu1,2,3 (AUTHOR) ; Wu, Hao1,2,3 (AUTHOR)
- المصدر:
Orphanet Journal of Rare Diseases. 2/21/2022, Vol. 17 Issue 1, p1-9. 9p.
No Comments.