Jun Yang

发表

Chromosome 22 LD map comparison between Korean and other populations

Y. J. Kim, Kyoung Oak Choi, B. Han, 2008 .

A genome-wide association study reveals association between common variants in an intergenic region of 4q25 and high-grade myopia in the Chinese Han population.

Tao Li, Lin He, Yongyong Shi, 2011, Human molecular genetics.

Polyalanine repeat expansion mutation of the HOXD13 gene in a Chinese family with unusual clinical manifestations of synpolydactyly.

Binbin Wang, Jing Wang, Xu Ma, 2011, European journal of medical genetics.

A novel mutation in a Chinese family with autosomal recessive Alport syndrome: a case report.

P. Han, Xuewen Yu, M. Shao, 2019, International journal of clinical and experimental pathology.

A commonly carried genetic variant, rs9616915, in SHANK3 gene is associated with a reduced risk of autism spectrum disorder: replication in a Chinese population

Ranran Song, Sanqing Xu, Zhao Sun, 2014, Molecular Biology Reports.

Juvenile bilateral lens dislocation and glaucoma associated with a novel mutation in the fibrillin 1 gene.

M. Pericak-Vance, M. Hauser, M. McDonald, 2006, Molecular vision.

A Synonymous Variant c.579A>G in the ETFDH Gene Caused Exon Skipping in a Patient With Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Case Report

Wei Zhou, Zhanjun Jia, B. Zheng, 2020, Frontiers in Pediatrics.

Exome Sequencing Identified NRG3 as a Novel Susceptible Gene of Hirschsprung’s Disease in a Chinese Population

X. Miao, R. Zhong, J. Ke, 2013, Molecular Neurobiology.

A commonly carried genetic variant, rs9616915, in SHANK3 gene is associated with a reduced risk of autism spectrum disorder: replication in a Chinese population

Ranran Song, Sanqing Xu, Zhao Sun, 2014, Molecular Biology Reports.

A novel non-synonymous mutation in the homeodomain of HOXD13 causes synpolydactyly in a Chinese family.

Xueya Zhou, Binbin Wang, Longfei Cheng, 2012, Clinica chimica acta; international journal of clinical chemistry.

Differences in frequencies of UGT1A9, 1A7, and 1A1 genetic polymorphisms in Chinese Tibetan versus Han Chinese populations.

Meilin Wang, F. Yang, X. Zhang, 2013, Genetics and molecular research : GMR.