G. Feng

The Novel Gene Locus for Agenesis of Permanent Teeth (He-Zhao deficiency) Maps to Chromosome 10q11.2

Y. Zhao, W. Huang, W. Liu, 2001, Journal of dental research.

A novel heterozygous nonsense mutation of keratin 5 in a chinese family with Dowling–Degos disease

L. He, X. Luo, J. Xuan, 2012, Journal of the European Academy of Dermatology and Venereology : JEADV.

Congenital absence of permanent teeth in a six-generation Chinese kindred.

W. Liu, S. Jiang, S. Li, 2000, American journal of medical genetics.

A novel DFNA5 mutation, IVS8+4 A>G, in the splice donor site of intron 8 causes late‐onset non‐syndromic hearing loss in a Chinese family

S. Z. Yang, D. Yan, G. Feng, 2007, Clinical genetics.

A locus for brachydactyly type A-1 maps to chromosome 2q35-q36.

G. Feng, Xiaoliu Shi, J. Guo, 2000, American journal of human genetics.

Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families

S. Z. Yang, D. Yan, G. Feng, 2008, Clinical genetics.