Fengling Song

Generation of an induced pluripotent stem cell line (SDQLCHi003-a) from a patient with short rib-thoracic dysplasia syndrome type III carrying compound heterozygous mutations in DYNC2H1.

Z. Gai, Yuqiang Lv, Min Gao, 2019, Stem cell research.

Chromosome r(3)(p25.3q29) in a Patient with Developmental Delay and Congenital Heart Defects: A Case Report and a Brief Literature Review

Z. Gai, Kaihui Zhang, Yi Liu, 2016, Cytogenetic and Genome Research.

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.

Genotypic and phenotypic characteristics of 12 chinese children with glycogen storage diseases

Z. Gai, Dong Wang, Kaihui Zhang, 2022, Frontiers in Genetics.

DCX variants in two unrelated Chinese families with subcortical band heterotopia: Two case reports and review of literature

Z. Gai, Yuqiang Lv, Jian Ma, 2023, Heliyon.