Shu-juan Song

发表

A case-control study of the association between tooth-development gene polymorphisms and non-syndromic hypodontia in the Chinese Han population.

Haochen Liu, H. Feng, Dong Han, 2012, European journal of oral sciences.

Novel EDA mutation resulting in X-linked non-syndromic hypodontia and the pattern of EDA-associated isolated tooth agenesis.

H. Feng, H. Qu, Xiao-xia Zhang, 2008, European journal of medical genetics.

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.

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.

WNT10A variants are associated with non-syndromic tooth agenesis in the general population

R. Zhao, Huiying He, Hailan Feng, 2013, Human Genetics.

A novel PAX6 gene mutation in a Chinese family with aniridia.

Ling-song Li, Shuling Wang, Ying-zhi Liu, 2005, Molecular vision.

Deletion of exon 4 in LAMA2 is the most frequent mutation in Chinese patients with laminin α2-related muscular dystrophy

R. Du, Ling Zhang, Yuwu Jiang, 2018, Scientific Reports.

Mutation frequency for Charcot-Marie-Tooth disease type 1 in the Chinese population is similar to that in the global ethnic patients

Ming Yan, Biao Chen, N. Zhong, 2006, Genetics in Medicine.

Female-Associated DNA Polymorphisms of Hemp (Cannabis sativa L.)

R. Clarke, Hong Shao, Shu-juan Song, 2003 .

Mutation analysis of PAX6 gene in a large Chinese family with aniridia.

Zhi-zhong Ma, Z. Hou, Ying Jin, 2005, Chinese Medical Journal.