Xueming Liu

MITF Is Mutated in Type 1 Waardenburg Syndrome With Unusual Phenotype

Yong Feng, L. Mei, Hongsheng Chen, 2020, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China

Q. Pan, Yong Feng, L. Mei, 2016, PloS one.

New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing

D. Yan, Yong Feng, L. Mei, 2019, Neural plasticity.

Mechanism underlying synergic activation of Tyrosinase promoter by MITF and IRF4

Yong Feng, L. Mei, Chufeng He, 2017 .

Waardenburg syndrome type II: phenotypic findings and diagnostic criteria.

A. Read, V. Newton, X. Liu, 1995, American journal of medical genetics.

Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IB.

K. Steel, A. Munnich, C. Petit, 1997, Human molecular genetics.