Wanyu Fu

Identification of partial trisomy 13q in two unrelated patients using single-nucleotide polymorphism array and literature overview

Chunnuan Chen, Yingjun Xie, Yuying Jiang, 2022, Molecular cytogenetics.

Application of the BACs-on-Beads assay for the prenatal diagnosis of chromosomal abnormalities in Quanzhou, China

Chunnuan Chen, Chunling Lv, Yuying Jiang, 2021, BMC Pregnancy and Childbirth.

A de novo PAK1 likely pathogenic variant and a de novo terminal 1q microdeletion in a Chinese girl with global developmental delay, severe intellectual disability, and seizures

Chunnuan Chen, Yingjun Xie, Yuying Jiang, 2023, BMC Medical Genomics.

Cytogenetic and molecular analysis of distal 4q duplication with distinctive phenotype using single-nucleotide polymorphism array

Yingjun Xie, Yuying Jiang, Shuhong Zeng, 2021, Molecular cytogenetics.

Topic Discovery and Topic-Driven Clustering for Audit Method Datasets

Shaobin Huang, Ying Zhao, Wanyu Fu, 2011, ADMA.

Sub-Exome Target Sequencing in a Family With Syndactyly Type IV Due to a Novel Partial Duplication of the LMBR1 Gene: First Case Report in Fujian Province of China

Hui Huang, Jing Wu, Lijing Shi, 2020, Frontiers in Genetics.

A familial case of Syndactyly type IV due to a novel duplication of ~222.23 kb covering exons 2-17 of the LMBR1 gene: a case report

Hui Huang, Jing Wu, Lijing Shi, 2018, bioRxiv.