Wei-Liang Liu
2PUBLICATIONS
0CO-AUTHORS
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Publications (2)
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|Jan 15, 2025
VPS13D-related disorders: a severe case, review, and genotype-phenotype correlation.Wei-Liang Liu, Fang Li
|Sep 22, 2023
"Liu-Liang-Chung" syndrome with multiple congenital anomalies and the distinctive craniofacial features caused by dominant ZEB2 gene gain mutation.Wei-Liang Liu, Fang Li, Wei Chen
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