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Molecular Genetics & Genomic Medicine|January 9, 2026
Identification of a Novel Likely Pathogenic Variant of DIAPH3 Associated With New Phenotype of Sensorineural Hearing LossLingling Zeng, Qiuchen Zheng, Xiedong Wu, et al.
Human Genetics|December 28, 2022
Quantitative assessment of low-level parental mosaicism of SNVs and CNVs in Waardenburg syndromeXiaohong Li, Shasha Huang, Guojian Wang, et al.
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