Search Results - Xuelian He

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  1. 1
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    A Heterozygous Novel Mutation in TFAP2A Gene Causes Atypical Branchio-Oculo-Facial Syndrome With Isolated Coloboma of Choroid: A Case Report by Jie Min, Bing Mao, Yong Wang, Xuelian He, Shuyang Gao, Hairong Wang

    Published 2020
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  2. 2
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    Severe congenital microcephaly with 16p13.11 microdeletion combined with NDE1 mutation, a case report and literature review by Li Tan, Bo Bi, Peiwei Zhao, Xiaonan Cai, Chunhui Wan, Jianbo Shao, Xuelian He

    Published 2017
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    The potential of 1.5 T magnetic resonance imaging for the evaluation of fetal anomalies of the great vessels by Linjun Xie, Hong Xu, Xuelian He, Hang Fu, Lu Zhang, Wei Bai, Xuesheng Li, Li Bao, Huayan Xu, Xiaohong Li, Yingkun Guo

    Published 2023
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    Activated phosphoinositide 3-kinase δ syndrome caused by PIK3CD mutations: expanding the phenotype by Peiwei Zhao, Juan Huang, Huicong Fu, Jiali Xu, Tianhong Li, Xiankai Zhang, Qingjie Meng, Lei Zhang, Li Tan, Wen Zhang, Hebin Chen, Xiaoxia Lu, Yan Ding, Xuelian He

    Published 2024
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