Yali Yang

Chromosomal microarray analysis of 410 Han Chinese patients with autism spectrum disorder or unexplained intellectual disability and developmental delay

S. Scherer, E. Higginbotham, M. Zarrei, 2022, NPJ genomic medicine.

Uniparental Disomy of Chromosome 15 in Two Cases by Chromosome Microarray: A Lesson Worth Thinking

Shu Liu, Z. Gai, Kaihui Zhang, 2017, Cytogenetic and Genome Research.

Clinical characteristics and mutation analysis of five Chinese patients with maple syrup urine disease

Z. Gai, Qing Gao, Kaihui Zhang, 2018, Metabolic Brain Disease.

Familial intellectual disability as a result of a derivative chromosome 22 originating from a balanced translocation (3;22) in a four generation family

Y. Huang, Z. Gai, Kaihui Zhang, 2018, Molecular Cytogenetics.

Clinical Application of an Innovative Multiplex-Fluorescent-Labeled STRs Assay for Prader-Willi Syndrome and Angelman Syndrome

Shu Liu, N. Jana, Z. Gai, 2016, PloS one.

[Analysis of CANT1 gene variant in a girl with Desbuquois dysplasia type I].

Y. Huang, Z. Gai, Kaihui Zhang, 2019, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Correction to: Familial intellectual disability as a result of a derivative chromosome 22 originating from a balanced translocation (3;22) in a four generation family

Z. Gai, Kaihui Zhang, Yi Liu, 2018, Molecular Cytogenetics.