Chuan Yu

Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP

Zhu Chen, Xiangyin Kong, G. Fu, 2001, Nature Genetics.

A 3-nucleotide deletion in the polypyrimidine tract of intron 7 of the DFNA5 gene causes nonsyndromic hearing impairment in a Chinese family.

Xiangyin Kong, Landian Hu, Xiangming Meng, 2003, Genomics.

The gamma S-crystallin gene is mutated in autosomal recessive cataract in mouse.

Xiangyin Kong, Q. Xie, L. Bu, 2002, Genomics.