Jianfan Chen

A female carrier of a novel DMD mutation with slightly skewed X-chromosome inactivation shows a suspected case of Becker muscular dystrophy in a Chinese family

Jian Wang, Fei He, F. Xiong, 2021, Molecular Genetics and Genomics.

Infant death from glutaric aciduria type IIc

Dongri Li, S. Du, F. Xiong, 2021, Forensic Science International: Reports.

The gain-of-function FAM83H mutation caused hypocalcification amelogenesis imperfecta in a Chinese family

Fei He, Yingchun Zheng, J. Xiong, 2020, Clinical Oral Investigations.

Genetic diagnosis of polycystic kidney disease, Alport syndrome, and thalassemia minor in a large Chinese family.

Xiangmin Xu, Xuelian Zhang, J. Xiong, 2017, Clinical science.

Double heterozygous pathogenic mutations in KIF3C and ZNF513 cause hereditary gingival fibromatosis

S. Chen, Shun-Lai Ma, Fei He, 2023, International journal of oral science.