B. Bai

Mutations in WNT10B Are Identified in Individuals with Oligodontia.

Zhongsheng Sun, Jinchen Li, Dong Han, 2016, American journal of human genetics.

Novel missense mutations in the AXIN2 gene associated with non-syndromic oligodontia.

Dong Han, Haochen Liu, Yixiang Wang, 2014, Archives of oral biology.

Involvement of and Interaction between WNT10A and EDA Mutations in Tooth Agenesis Cases in the Chinese Population

Zhenting Zhang, Huiying He, H. Qu, 2013, PloS one.

Nine Novel PAX9 Mutations and a Distinct Tooth Agenesis Genotype-Phenotype

H. Feng, X. Zhang, B. Bai, 2018, Journal of dental research.

Correlation between the phenotypes and genotypes of X-linked hypohidrotic ectodermal dysplasia and non-syndromic hypodontia caused by ectodysplasin-A mutations.

H. Feng, S. Pan, Dong Han, 2011, European journal of medical genetics.

4q27 as a psoriasis susceptibility locus in the Northeastern Chinese Han population.

P. Xu, F. Wang, J. Zhou, 2015, Tissue antigens.

Mutations in WNT10B Are Identified in Individuals with Oligodontia.

Zhongsheng Sun, Jinchen Li, H. Feng, 2016, American journal of human genetics.

Novel missense mutations in the AXIN2 gene associated with non-syndromic oligodontia.

Haochen Liu, Yixiang Wang, H. Feng, 2014, Archives of oral biology.