Haiyan Yang
2PUBLICATIONS
0CO-AUTHORS
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Publications (2)
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|May 31, 2022
ARHGEF9 gene variant leads to developmental and epileptic encephalopathy: Genotypic phenotype analysis and treatment exploration.Haiyan Yang, Hongmei Liao, Siyi Gan
|Jan 29, 2022
Exon skipping caused by a complex structural variation in SH2D1A resulted in X-linked lymphoproliferative syndrome type 1.Liwen Wu, Feng Yang, Jia Wang
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