Malformations of cortical development: Fetal imaging and geneticsL. Wang, Aihua Yin, Dahua Meng et al.|Molecular Genetics & Genomic Medicine|2024Cited by 10
Clinical and molecular analysis of Guangxi patients with Kabuki syndrome and KMT2D mutationsSheng Yi, Jingsi Luo, Xiaofei Zhang et al.|Heliyon|2023Cited by 4
A genetic variant in the <i>MAST1</i> gene is associated with mega‐corpus‐callosum syndrome with hypoplastic cerebellar vermis, in a fetusSheng Yi, Jingsi Luo, Xianglian Tang et al.|Molecular Genetics & Genomic Medicine|2024Cited by 4
Novel and recurrent ASPM mutations of founder effect in Chinese populationMengting Li, Yiping Shen, Jingrong Luo et al.|Brain and Development|2022Cited by 2