Proximal 4p Deletion Syndrome in an Infant With Multiple Systemic AnomaliesYing Pang, Shuyao Zhu, Guanghuan Pi et al.|Molecular Genetics & Genomic Medicine|2024Cited by 2
Genotype-phenotype correlation of ODLURO syndrome comorbid epilepsy associated with KMT2E variations: Report on a novel case and systematic literature reviewShuyao Zhu, Ai Chen, Lan Zeng et al.|Epilepsy & Behavior|2025Cited by 2
Genetic analysis of partial duplication of the long arm of chromosome 16Dan Tang, Shuyao Zhu, Jun Hui Fan et al.|BMC Medical Genomics|2024Cited by 1
Prenatal diagnosis of monozygotic twins with phenotypic differences in chromosome 17q12 deletion syndromeDan Ma, Shuyao Zhu, Tao Yuan et al.|Journal of Clinical Ultrasound|2024Cited by 0