Hasil Pencarian - Yu'e Chen
- Menampilkan 1 - 14 hasil dari 14
-
1
Toxicokinetic modeling challenges for aquatic nanotoxicology oleh Wei-Yu eChen
Diterbitkan 2016-01-01
Artikel -
2
-
3
Prenatal diagnosis and molecular cytogenetic characterization of fetuses with central nervous system anomalies using chromosomal microarray analysis: a seven-year single-center ret... oleh Jianlong Zhuang, Na Zhang, Yu’e Chen, Yuying Jiang, Xinying Chen, Wenli Chen, Chunnuan Chen
Diterbitkan 2024-01-01
Artikel -
4
-
5
-
6
Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication oleh Jianlong Zhuang, Chunnuan Chen, Yuanbai Wang, Shuhong Zeng, Yu’e Chen, Yuying Jiang, Yingjun Xie, Yingjun Xie, Gaoxiong Wang
Diterbitkan 2022-07-01
Artikel -
7
Etiological identification of recurrent male fatality due to a novel NSDHL gene mutation using trio whole‐exome sequencing: A rare case report and literature review oleh Jianlong Zhuang, Qi Luo, Meihua Xie, Yu’e Chen, Yuying Jiang, Shuhong Zeng, Yuanbai Wang, Yingjun Xie, Chunnuan Chen
Diterbitkan 2023-03-01
Artikel -
8
Catalytic Degradation of Triphenylmethane Dyes with an Iron Porphyrin Complex as a Cytochrome P450 Model oleh Xiaoyan Lu, Qiman Che, Xinkai Niu, Yilin Zhang, Yu’e Chen, Qing Han, Miaoqing Li, Shuang Wang, Jihong Lan
Diterbitkan 2023-07-01
Artikel -
9
The Genetic Etiology Diagnosis of Fetal Growth Restriction Using Single-Nucleotide Polymorphism-Based Chromosomal Microarray Analysis oleh Yu'e Chen, Yingjun Xie, Yingjun Xie, Yuying Jiang, Qi Luo, Lijing Shi, Shuhong Zeng, Jianlong Zhuang, Guorong Lyu
Diterbitkan 2021-10-01
Artikel -
10
Identification of a Rare Variant of c.1777G>A (p.G593S) in the COL1A1 Gene as the Etiology of Recurrent Osteogenesis Imperfecta by Whole-Exome Sequencing oleh Jianlong Zhuang, Chunnuan Chen, Yu'e Chen, Qi Luo, Yuanbai Wang, Yuying Jiang, Shuhong Zeng, Yingjun Xie, Yingjun Xie, Dongmei Chen
Diterbitkan 2022-04-01
Artikel -
11
Case Report: Prenatal Diagnosis of a Novel Variant c.251dupT (p.N87Kfs*6) in BCOR Resulting in Oculofaciocardiodental Syndrome Using Whole-Exome Sequencing oleh Jianlong Zhuang, Chunnuan Chen, Yu’e Chen, Shuhong Zeng, Yuying Jiang, Yuanbai Wang, Xinying Chen, Yingjun Xie, Yingjun Xie, Gaoxiong Wang
Diterbitkan 2022-03-01
Artikel -
12
-
13
Effect of different application duration of a venous foot pump on prevention of venous thromboembolism after hip and knee arthroplasty: a multicenter prospective clinical trial oleh Siqi Gu, Yu-e Chen, Mingxing Lei, Jiahui Li, Wanying Li, Meihong Zhang, Hongxia Zhu, Mengying Ma, Dan Kong, Yuan Gao
Diterbitkan 2023-12-01
Artikel -
14
Case Report: Novel compound heterozygous variants in CHRNA1 gene leading to lethal multiple pterygium syndrome: A case report oleh Jianlong Zhuang, Junyu Wang, Qi Luo, Shuhong Zeng, Yu’e Chen, Yuying Jiang, Xinying Chen, Yuanbai Wang, Yingjun Xie, Yingjun Xie, Gaoxiong Wang, Chunnuan Chen
Diterbitkan 2022-08-01
Artikel