Mei Yang
7PUBLICATIONS
5CO-AUTHORS
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Publications (7)
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|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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