L. Pan

Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegia

Zhi-ying Wu, Qiao Wei, Hong-Fu Li, 2019, Translational Neurodegeneration.

Molecular diagnosis for 55 fetuses with skeletal dysplasias by whole‐exome sequencing: A retrospective cohort study

D. Liang, Zhuo Li, Lingqian Wu, 2021, Clinical genetics.

Novel GZF1 pathogenic variants identified in two Chinese patients with Larsen syndrome

D. Liang, Zhuo Li, Lingqian Wu, 2020, Clinical genetics.

Clinical data and genetic mutation in Kallmann syndrome with CHARGE syndrome

Xuan Xu, L. Pan, Jiang Wang, 2018, Medicine.

Genetic basis of glycogen storage disease type 1a: prevalent mutations at the glucose-6-phosphatase locus.

Yuan-Tsong Chen, J. Liu, J. V. Van Hove, 1995, American journal of human genetics.

Chromosome Analysis and Postnatal Follow-Up of Fetuses With Abnormal Ultrasound Findings

Zhenhui Zhang, L. Pan, Lei Dai, 2021 .

Mutations in the glucocerebrosidase gene are responsible for Chinese patients with Parkinson’s disease

F. Han, W. Le, Zhe Yu, 2014, Journal of Human Genetics.

Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegia

Qiao Wei, Hong-Fu Li, Zhi-Jun Liu, 2019, Translational Neurodegeneration.