X. Kong

Clinical and molecular characteristics of thirty NF1 variants in Chinese patients with neurofibromatosis type 1

Wen Wang, Weibing Qin, Hongsong Ge, 2019, Molecular Biology Reports.

Next‐generation sequencing through multi‐gene panel testing for diagnosis of hereditary ichthyosis in Chinese

X. Kong, Ming Li, Z. Yao, 2020, Clinical genetics.

Clinical and molecular characteristics of thirty NF1 variants in Chinese patients with neurofibromatosis type 1

Wen Wang, Weibing Qin, Hongsong Ge, 2019, Molecular Biology Reports.

A new locus for hereditary gingival fibromatosis (GINGF2) maps to 5q13-q22.

X. Kong, M. Yang, L. Bu, 2001, Genomics.

Coinheritance of generalized pustular psoriasis and familial Behçet‐like autoinflammatory syndrome with variants in IL36RN and TNFAIP3 in the heterozygous state

X. Kong, Ming Li, Hui Zhang, 2019, The Journal of dermatology.

Case Report: Chanarin-Dorfman Syndrome: A Novel Homozygous Mutation in ABHD5 Gene in a Chinese Case and Genotype-Phenotype Correlation Analysis

X. Kong, Peiguang Wang, Hervé Huang, 2022, Frontiers in Genetics.