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Molecular Genetics & Genomic Medicine|December 11, 2023
Exome sequencing-aided precise diagnosis of four families with type I Stickler syndromeRunyi Tian, Ping Tong, Yuhong He, et al.International Journal of Molecular Sciences|August 28, 2025
Bi-Allelic Loss-of-Function Variant in MAN1B1 Cause Rafiq Syndrome and Developmental DelayLiyu Zang, Yaoling Han, Qiumeng Zhang, et al.Journal of Medical Genetics|October 18, 2023
CCDC66 mutations are associated with high myopia through affected cell mitosisXiaozhen Chen, Ping Tong, Ying Jiang, et al.Pageof 1