Wen-huai Xu

Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients

I. Ellis, L. Aaltonen, D. Evans, 1999, Journal of medical genetics.

Whole-exome sequencing identified compound heterozygous variants in MMKS in a Chinese pedigree with Bardet-Biedl syndrome

Zhan Qi, Qian Fu, Ying Shen, 2017, Science China Life Sciences.

Genetic diagnostic yields of 354 Chinese ASD children with rare mutations by a pipeline of genomic tests

Chanjuan Hao, Yueming Zhang, Xuanshi Liu, 2023, Frontiers in Genetics.

Whole-exome sequencing identified compound heterozygous variants in MMKS in a Chinese pedigree with Bardet-Biedl syndrome

Qian Fu, Wei Li, Zhan Qi, 2017, Science China Life Sciences.