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Mei Yang

7PUBLICATIONS

5CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)NeurogeneticsNeonatologyMedical mycology

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Publications (7)

Sort by Publication Date:

|Sep 26, 2024

Screening a new set of microhaplotypes in exonic regions for sample identity testing and paternity testing during whole exome sequencing analysis.

Yu Tan, Huan Tian, Yuanyuan Xiao

|Nov 10, 2023

A case of congenital cataracts with hypotrichosis caused by compound heterozygous variants in the LSS gene.

Yu Tan, Huan Tian, Jingqun Mai

|Nov 06, 2023

Identification of a novel LMX1B nonsense variant associated with congenital talipes equinovarus by prenatal exome sequencing: A case report.

Jing Chen, Qinqin Xiang, Xiao Xiao

|Jun 05, 2023

A novel heterozygous PKD1 variant causing alternative splicing in a Chinese family with autosomal dominant polycystic kidney disease.

Qianying Zhao, Yu Tan, Xiao Xiao

|Dec 20, 2022

Compound heterozygous splicing variants in KIAA0586 cause fetal short-rib thoracic dysplasia and cerebellar malformation: Use of exome sequencing in prenatal diagnosis.

Qianying Zhao, Bocheng Xu, Qinqin Xiang

|Aug 01, 2022

A novel CLCNKB variant in a Chinese family with classic Bartter syndrome and prenatal genetic diagnosis.

Qianying Zhao, Qinqin Xiang, Yu Tan

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Frequent Collaborators

3 joint publications

Qianying Zhao

1 joint publications

Yanyan Liu

1 joint publications

Huaqin Sun

1 joint publications

Ting Hu

1 joint publications

Yu Tan

Frequent Collaborators

3 joint publications

Qianying Zhao

1 joint publications

Yanyan Liu

1 joint publications

Huaqin Sun

1 joint publications

Ting Hu

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