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ArticleBMC pediatrics2023

"Liu-Liang-Chung" syndrome with multiple congenital anomalies and the distinctive craniofacial features caused by dominant ZEB2 gene gain mutation.

Wei-Liang Liu et al.PubMed ↗Full text ↗Publisher ↗

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1 paper cites it

2023
2024
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Full record →Abstract, authors, funding and every citing paper · PMID 37735378