Xinhua Bao

3PUBLICATIONS
0CO-AUTHORS
Gene and molecular therapyGene expression (incl. microarray and other genome-wide approaches)Cancer genetics
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Publications (3)

|Nov 01, 2018
Novel MEF2C point mutations in Chinese patients with Rett (-like) syndrome or non-syndromic intellectual disability: insights into genotype-phenotype correlation.

Jiaping Wang, Qingping Zhang, Yan Chen

|Sep 20, 2017
SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures.

Jiaping Wang, Hua Gao, Xinhua Bao

|Aug 31, 2017
Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation.

Qingping Zhang, Jiaping Wang, Jiarui Li

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