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Author

Yu Han

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Case report Aug 2026

[Clinical and genetic analysis of a child with MRXS34 syndrome due to variant of NONO gene].

A literature review showed that, among 23 BVSYS patients reported between 2015 and 2025, the most common clinical manifestations were developmental delay/intellectual disability and characteristic facial features, followed by speech impairment and characteristic facial features, and cardiac anomalies.

Yong Zhao, Nuo Li, Yu Han et al. · 0 citations

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