Ruolan Guo

A clear bias in parental origin of de novo pathogenic CNVs related to intellectual disability, developmental delay and multiple congenital anomalies

Jing Guo, Desheng Liang, Lingqian Wu, 2017, Scientific Reports.

Compound heterozygous variants in POR gene identified by whole‐exome sequencing in a Chinese pedigree with cytochrome P450 oxidoreductase deficiency

Wei Li, Zhan Qi, Zhan Qi, 2018, Pediatric investigation.