Juan Yang

发表

Dynamic mutation analysis of a SCA3 Chinese Han family and prenatal diagnosis

C. Zhang, Fei Chen, Jing Li, 2012 .

Clinical Pictures and Novel Mutations of WT1-Associated Denys–Drash Syndrome in Two Chinese Children

Yuanyuan Pei, K. Lai, Xiaoyun Jiang, 2011, Renal failure.

A novel uromodulin mutation in autosomal dominant tubulointerstitial kidney disease: a pedigree-based study and literature review

Tao Chen, Yerong Yu, Z. An, 2018, Renal failure.

Tyrosine-protein phosphatase nonreceptor type 12 is a novel prognostic biomarker for esophageal squamous cell carcinoma.

M. Zeng, Z. Wen, R. Luo, 2012, The Annals of thoracic surgery.

Serum Creatinine Distinguishes Duchenne Muscular Dystrophy from Becker Muscular Dystrophy in Patients Aged ≤3 Years: A Retrospective Study

Juan Yang, Ji⁃qing Cao, Liang Wang, 2017, Front. Neurol..

MLPA-based genotype–phenotype analysis in 1053 Chinese patients with DMD/BMD

Fei Chen, Shao-ying Li, Jing Li, 2013, BMC Medical Genetics.

The absence of dystrophin rather than muscle degeneration causes acetylcholine receptor cluster defects in dystrophic muscle

Qiuling Li, Fei Chen, Juan Yang, 2012, Neuroreport.

Hereditary motor and sensory neuropathy with SOD1-mutant: A case report

Linhai Zhang, Zhong Luo, Juan Yang, 2022, Medicine.

Association of PTPN22-C1858T Polymorphism With Susceptibility to Mycobacterium tuberculosis and Mycobacterium leprae Infection: A Meta-Analysis

Z. Zhao, Zhihua Zheng, Yun Chen, 2021, Frontiers in Immunology.

Prenatal diagnosis and genetic analysis of a fetus with Branchio-oto-renal syndrome: A case report

Juan Yang, Ping Tang, Jun Li, 2022, Medicine.

WT1 mutation-associated nephropathy: a single-center experience .

Yulin L. Liu, Juan Yang, Ting Liu, 2017, Clinical nephrology.

Clinical characteristics and gene mutation analysis of riboflavin-responsive lipid storage myopathy: report of 3 cases in 2 families and review of literature

Ying-yin Liang, J. Geng, Jing Li, 2014 .