Associated Papers
Targeted sequencing identifies 33 novel mutations in 130 ClinGen curated hearing loss genes among 253 pediatric patients: A retrospective case study.
Zhou Z et al.
Biomedical Reports, 2025
[Application of next generation sequencing in 3 Waardenburg syndrome].
Xu B et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery, 2021
Identification of six novel variants in Waardenburg syndrome type II by next-generation sequencing.
Ren S et al.
Molecular Genetics & Genomic Medicine, 2020
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