1. Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
   Guangmin Chen et al, 2021, Frontiers in Genetics CrossRef
2. Two novel mutations of PAX3 and SOX10 were characterized as genetic causes of Waardenburg Syndrome
   Yongbo Yu et al, 2020, Molecular Genetics & Genomic Medicine CrossRef
3. Targeted Next-Generation Sequencing Identifies Separate Causes of Hearing Loss in One Deaf Family and Variable Clinical Manifestations for the p.R161C Mutation inSOX10
   Xiaoyu Yu et al, 2020, Neural Plasticity CrossRef
4. A Novel Spontaneous Mutation of the SOX10 Gene Associated with Waardenburg Syndrome Type II
   Sen Chen et al, 2020, Neural Plasticity CrossRef