Wen Jiang

Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II

K. Xia, Yong Feng, L. Mei, 2011, Human Genetics.

Novel mutations in the SOX10 gene in the first two Chinese cases of type IV Waardenburg syndrome.

K. Xia, Zhengmao Hu, Yong Feng, 2011, Biochemical and biophysical research communications.

Paternal origin of FGFR2 mutations in sporadic cases of Crouzon and Pfeiffer syndromes.

E. Jabs, Diana S. Johnson, S. Boyadjiev, 1999 .

Prenatal ultrasonographic and molecular diagnosis of apert syndrome

E. Jabs, K. Filkins, Wen Jiang, 1997, Prenatal diagnosis.

Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II

K. Xia, Yong Feng, L. Mei, 2012, Human Genetics.

Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndrome.

Rivka L. Glaser, E. Jabs, A. Wilkie, 2000, American journal of human genetics.