Chao Gao
Children’s Hospital Affiliated with Zhengzhou University
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[Two novel RUNX2 gene mutations in two Chinese families with cleidocranial dysplasia].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics Apr, 2010 | Pubmed ID: 20376792
The correlation between AGT gene polymorphism and neonatal hypoxic-ischemic encephalopathy (HIE).
European review for medical and pharmacological sciences Mar, 2019 | Pubmed ID: 30915766
[Clinical and genetic analysis of a Chinese pedigree affected with Smith-Lemli-Opitz syndrome].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics Nov, 2020 | Pubmed ID: 33179238
[Compound heterozygous NDUFS1 variants identified in a Chinese pedigree affected with mitochondrial respiratory chain complex I deficiency].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics Mar, 2021 | Pubmed ID: 33751534
The GluN2B-Trp373 NMDA Receptor Variant is Associated with Autism-, Epilepsy-Related Phenotypes and Reduces NMDA Receptor Currents in Rats.
Neurochemical research Jun, 2022 | Pubmed ID: 35181828
Paternal uniparental disomy of chromosome 16 resulting in homozygosity of a GPT2 mutation causes intellectual and developmental disability.
European journal of medical genetics Sep, 2022 | Pubmed ID: 35793769
[Clinical characteristics and genetic variant analysis of a child with Snijders Blok-Campeau syndrome].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics Apr, 2023 | Pubmed ID: 36972932
