Vulto-van Silfhout-de Vries syndrome caused by de novo variants of DEAF1 gene: a case report and literature reviewHui Zhu, Zemin Luo, Yu Huang et al.|Frontiers in Neurology|2023Cited by 6
Expanding the phenotypic spectrum of Rauch-Steindl syndrome: A novel NSD2 variant with atrial septal defect in a Chinese patientHui Zhu, Zemin Luo, Min Du et al.|Research Square|2025Cited by 0