Xiaoli Chen
7PUBLICATIONS
10CO-AUTHORS
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Publications (7)
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|Jul 29, 2025
Alu-mediated FANCD2 exonic deletion contributes to Fanconi anaemia.Shaofang Shangguan, Xinyuan Cui, Juanjuan Li
|Jul 30, 2024
A novel compound heterozygous mutation of UFC1 in a patient with neurodevelopmental disorder.Ye Han, Yangyang Ge, Haoran Liu
|May 05, 2021
Confirming the contribution and genetic spectrum of de novo mutation in infantile spasms: Evidence from a Chinese cohort.Liying Liu, Fang Liu, Qiuhong Wang
|Jan 06, 2021
CNV profiles of Chinese pediatric patients with developmental disorders.Haiming Yuan, Shaofang Shangguan, Zhengchang Li
|Sep 02, 2020
Neurodevelopmental trajectory and modifiers of 16p11.2 microdeletion: A follow-up study of four Chinese children carriers.Hua Xie, Fang Liu, Yu Zhang
|Sep 11, 2019
A rare case of acquired immunodeficiency associated with myelodysplastic syndrome.Juanjuan Li, Junhui Li, Jianguo Li
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