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Plos One|May 31, 2017
Genomic structure, expression pattern, and functional characterization of transcription factor E2F-2 from black tiger shrimp (Penaeus monodon)Bobo Xie, Pengfei Wang, Chao Zhao, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|December 25, 2014
[ASS1 gene mutation in a neonate with citrullinemia type I]Bobo Xie, Rongyu Chen, Jin Wang, et al.
Fish & Shellfish Immunology|August 13, 2016
Cloning, characterization, and expression of the macrophage migration inhibitory factor gene from the black tiger shrimp (Penaeus monodon)Bobo Xie, Mingjun Fu, Chao Zhao, et al.
Molecular Genetics & Genomic Medicine|March 2, 2022
Phenotypic variability of syndromic craniosynostosis caused by c.833G > T in FGFR2: Clinical and genetic evaluation of eight patients from a five-generation familyXianda Wei, Guori Huang, Baoheng Gui, et al.
Frontiers in Pediatrics|January 21, 2026
Expansion of the genetic and phenotypic spectrum of hereditary spastic paraplegia caused by ABHD16A gene variants: an integrated analysis based on novel variants and literature reviewManling He, Qiang Zhang, Shaoke Chen, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 4, 2024
[Analysis of a child with DIGFAN syndrome due to variant of MORC2 gene]Bobo Xie, Xin Fan, Xianda Wei, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 10, 2016
[Identification of two novel mutations of MUT gene in a Chinese family affected with isolated methylmalonic acidemia]Bobo Xie, Jingsi Luo, Xin Fan, et al.
BMC Medical Genetics|May 1, 2015
EPHA4 haploinsufficiency is responsible for the short stature of a patient with 2q35-q36.2 deletion and Waardenburg syndromeChuan Li, Rongyu Chen, Xin Fan, et al.
Plos One|May 26, 2018
Genomic structure, expression, and functional characterization of checkpoint kinase 1 from Penaeus monodonLihua Qiu, Chao Zhao, Pengfei Wang, et al.
Scientific Reports|July 2, 2025
Genetic skeletal disorders: phenotypic-genotypic characteristics and RhGH therapy responses of a pediatric cohortYiyun Huang, Yan Peng, Chuan Li, et al.
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