Chao Gao

[Two novel RUNX2 gene mutations in two Chinese families with cleidocranial dysplasia].

The correlation between AGT gene polymorphism and neonatal hypoxic-ischemic encephalopathy (HIE).

[Clinical and genetic analysis of a Chinese pedigree affected with Smith-Lemli-Opitz syndrome].

[Compound heterozygous NDUFS1 variants identified in a Chinese pedigree affected with mitochondrial respiratory chain complex I deficiency].

The GluN2B-Trp373 NMDA Receptor Variant is Associated with Autism-, Epilepsy-Related Phenotypes and Reduces NMDA Receptor Currents in Rats.

Paternal uniparental disomy of chromosome 16 resulting in homozygosity of a GPT2 mutation causes intellectual and developmental disability.

[Clinical characteristics and genetic variant analysis of a child with Snijders Blok-Campeau syndrome].