Zhaoyan Meng

Detailed pedigree analyses and prenatal diagnosis for a family with mucopolysaccharidosis type II

Zongfu Cao, L. Hui, Chuan Zhang, 2021, BMC medical genomics.

Whole-exome sequencing identified a homozygous novel RAG1 mutation in a child with omenn syndrome.

S. Banerjee, B. Yi, Yanxia Wang, 2022, Allergologia et immunopathologia.

Identification of a novel ANK1 mutation in hereditary spherocytosis co‐existing with BWS

X. Wang, Chuan Zhang, Zhaoyan Meng, 2022, Molecular genetics & genomic medicine.

Novel de novo mutation in ZBTB20 in a Chinese Primrose syndrome family and a review of the literature.

Chuan Zhang, S. Hao, Zhaoyan Meng, 2023, Molecular genetics & genomic medicine.