Zhiqiang Wang

Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation.

Xiangyin Kong, Bin Cui, Yu Xia, 2009, American journal of human genetics.

Identification of a novel GPR143 deletion in a Chinese family with X-linked congenital nystagmus

Xiangyin Kong, Landian Hu, Zhiqiang Wang, 2008, Molecular vision.

Uncovering the Rare Variants of DLC1 Isoform 1 and Their Functional Effects in a Chinese Sporadic Congenital Heart Disease Cohort

Xiangyin Kong, G. Ning, Yuchao Zhang, 2014, PloS one.

A single C to T transition in intron 5 of LMBR1 gene is associated with triphalangeal thumb-polysyndactyly syndrome in a Chinese family.

Xiangyin Kong, Landian Hu, Yao-zhou Shi, 2007, Biochemical and biophysical research communications.