Shuwen He
2PUBLICATIONS
0CO-AUTHORS

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Publications (2)
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|Jan 29, 2025
Novel De Novo Intronic Variant of SYNGAP1 Associated With the Neurodevelopmental Disorders.Wuming Xie, Baoqiong Liao, Mei Shuai
|Jan 08, 2025
Identification of novel CDH23 heterozygous variants causing autosomal recessive nonsyndromic hearing loss.Baoqiong Liao, Wuming Xie, Rutian Liu
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