Fang Li

A novel gross deletion and breakpoint junction sequence analysis of ATP7B in a Chinese family with Wilson disease using next-generation sequencing and Sanger sequencing

Zhi-Xu He, Wei-Liang Liu, Fang Li, 2019, Molecular medicine reports.

Schinzel–Giedion syndrome: a novel case, review and revised diagnostic criteria

Zhi-Xu He, Wei-Liang Liu, Fang Li, 2018, Journal of Genetics.

Analysis of bilirubin UDP-glucuronosyltransferase gene mutations in an unusual Crigler-Najjar syndrome patient.

Wei-Liang Liu, Fang Li, R. Ai, 2012, Molecular medicine reports.

Identification of a case of glucose‐6‐phosphate dehydrogenase deficiency with G6PD mediterranean–middle east subtype in China

Fang Li, R. Ai, W-L Liu, 2013, International journal of laboratory hematology.

Schinzel–Giedion syndrome: a novel case, review and revised diagnostic criteria

Wei-Liang Liu, Fang Li, R. Ai, 2018, Journal of Genetics.

Glucose‐6‐phosphate dehydrogenase qingzhen: Identification of a novel splice mutation (IVS5‐1 G>A)

Wei-Liang Liu, Fang Li, R. Ai, 2012, Pediatric blood & cancer.

A novel case of natural killer cell deficiency associated with Joubert syndrome

Jing Huang, Wei-Liang Liu, Fang Li, 2013, The International journal of neuroscience.

“Liu-Liang-Chung” syndrome with multiple congenital anomalies and the distinctive craniofacial features caused by dominant ZEB2 gene gain mutation

Wei Chen, Fang Li, Wei Chen, 2023, BMC Pediatrics.