Vulto-van Silfhout-de Vries syndrome caused by de novo variants of DEAF1 gene: a case report and literature reviewHui Zhu, Zemin Luo, Lan Zeng et al.|Frontiers in Neurology|2023Cited by 6
Renal–hepatic–pancreatic dysplasia-1 with a novel NPHP3 genotype: a case report and review of the literatureHui Zhu, Jin Wang, Zhihui Zhao et al.|BMC Pediatrics|2022Cited by 5
Proximal 4p Deletion Syndrome in an Infant With Multiple Systemic AnomaliesYing Pang, Shuyao Zhu, Lan Zeng et al.|Molecular Genetics & Genomic Medicine|2024Cited by 2
Dual diagnosis of microcephalic osteosplastic primary dwarfism type II and benign familial infantile seizure type 2: a case reportShuyao Zhu, Lan Zeng, Jin Wang et al.|Clinical Dysmorphology|2024Cited by 1