Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Human Mutation|April 14, 2025
Genome Sequencing Unveils the Role of Copy Number Variants in Hearing Loss and Identifies Novel Deletions With Founder Effect in the DFNB1 LocusZibin Lin, Jiale Xiang, Xiangzhong Sun, et al.
Frontiers in Genetics|March 5, 2026
Novel LARS2 variants in patients with Perrault syndrome: expanding the genetic spectrum and phenotypic heterogeneityZibin Lin, Jiale Xiang, Xiangzhong Sun, et al.
Clinical Chemistry|May 19, 2023
The Next Generation of Population-Based DFNB16 Carrier Screening and Diagnosis: STRC Copy-Number Variant Analysis from Genome Sequencing DataJiale Xiang, Jiguang Peng, Xiangzhong Sun, et al.
Scientific Reports|July 9, 2025
Determining the origin of genome aberrations improves the positive predictive value of NIPT for 22q11.2 deletion syndromeJiale Xiang, Xiangzhong Sun, Jiguang Peng, et al.
Pageof 2