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| A Model of Waardenburg Syndrome Using Patient-Derived iPSCs With a SOX10 Mutation Displays Compromised Maturation and Function of the Neural Crest That … J Wen, J Song, Y Bai, Y Liu, X Cai, L Mei, L Ma, C He, Y Feng Frontiers in Cell and Developmental Biology 9, 720858, 2021 | 12 | 2021 |
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| Exome sequencing identifies a novel missense mutation of WFS1 as the cause of non-syndromic low-frequency hearing loss in a Chinese family Z Niu, Y Feng, Z Hu, J Li, J Sun, H Chen, C He, X Wang, L Jiang, Y Liu, ... International journal of pediatric otorhinolaryngology 100, 1-7, 2017 | 11 | 2017 |
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