Search Results - Hailong Huang

Genetic and ultrasonographic analyses of fetuses with 1q21.1q21.2 microdeletion/microduplication: a retrospective study by Nan Guo, Huili Xue, Bin Liang, Hailong Huang, Meiying Cai, Liangpu Xu

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Intrauterine ultrasound phenotyping, molecular characteristics, and postnatal follow-up of fetuses with the 15q11.2 BP1-BP2 microdeletion syndrome: a single-center, retrospective c... by Meiying Cai, Aixiang Lv, Wantong Zhao, Liangpu Xu, Na Lin, Hailong Huang

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Prenatal ultrasound phenotypic and genetic etiology of the 17q12 microduplication syndrome by Meiying Cai, Min Lin, Nan Guo, Meimei Fu, Liangpu Xu, Na Lin, Hailong Huang

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Evaluation of chromosomal abnormalities and copy number variations in fetuses with ultrasonic soft markers by Meiying Cai, Na Lin, Xuemei Chen, Meimei Fu, Nan Guo, Liangpu Xu, Hailong Huang

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Intraparenchymal Neural Stem/Progenitor Cell Transplantation for Ischemic Stroke Animals: A Meta-Analysis and Systematic Review by Hailong Huang, Kun Qian, Xiaohua Han, Xin Li, Yifeng Zheng, Zhishui Chen, Xiaolin Huang, Hong Chen

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16p13.11 microdeletion/microduplication in fetuses: investigation of associated ultrasound phenotypes, genetic anomalies, and pregnancy outcome follow-up by Meiying Cai, Yanting Que, Xuemei Chen, Yuqing Chen, Bin Liang, Hailong Huang, Liangpu Xu, Na Lin

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Fetal Aberrant Right Subclavian Artery: Associated Anomalies, Genetic Etiology, and Postnatal Outcomes in a Retrospective Cohort Study by Meiying Cai, Na Lin, Xiangqun Fan, Xuemei Chen, Shiyi Xu, Xianguo Fu, Liangpu Xu, Hailong Huang

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Chromosomal Abnormalities and Pregnancy Outcomes for Fetuses With Gastrointestinal Tract Obstructions by Xiaoqing Wu, Xiaoqing Wu, Xiaoqing Wu, Linjuan Su, Linjuan Su, Qingmei Shen, Qingmei Shen, Qun Guo, Qun Guo, Ying Li, Ying Li, Shiyi Xu, Na Lin, Na Lin, Hailong Huang, Hailong Huang, Liangpu Xu, Liangpu Xu

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Corrigendum: Chromosomal abnormalities and pregnancy outcomes for fetuses with gastrointestinal tract obstructions by Xiaoqing Wu, Xiaoqing Wu, Xiaoqing Wu, Linjuan Su, Linjuan Su, Qingmei Shen, Qingmei Shen, Qun Guo, Qun Guo, Ying Li, Ying Li, Shiyi Xu, Na Lin, Na Lin, Hailong Huang, Hailong Huang, Liangpu Xu, Liangpu Xu

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Clinical findings and genetic analysis of patients with copy number variants involving 17p13.3 using a single nucleotide polymorphism array: a single-center experience by Bin Liang, Donghong Yu, Wantong Zhao, Yan Wang, Xiaoqing Wu, Lingji Chen, Na Lin, Hailong Huang, Liangpu Xu

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Fetal genetic findings by chromosomal microarray analysis and karyotyping for fetal growth restriction without structural malformations at a territory referral center: 10-year expe... by Xiaoqing Wu, Shuqiong He, Ying Li, Danhua Guo, Xuemei Chen, Bin Liang, Meiying Wang, Hailong Huang, Liangpu Xu

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Integrated analysis of inflammatory response subtype-related signature to predict clinical outcomes, immune status and drug targets in lower-grade glioma by Yudong Cao, Hecheng Zhu, Quan Chen, Hailong Huang, Dongcheng Xie, Xuewen Li, Xingjun Jiang, Caiping Ren, Jiahui Peng

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Prenatal diagnosis of genetic aberrations in fetuses with pulmonary stenosis in southern China: a retrospective analysis by Meiying Cai, Nan Guo, Meimei Fu, Yuqing Chen, Bin Liang, Yanting Que, Qingqiang Ji, Hailong Huang, Liangpu Xu, Na Lin

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Ultrasonographic characteristics, genetic features, and maternal and fetal outcomes in fetuses with omphalocele in China: a single tertiary center study by Yanting Que, Meiying Cai, Fang Yang, Qingqiang Ji, Shuqi Zhang, Wenhui Huang, Yashi Gao, Bojing Zhou, Hailong Huang, Hua Cao, Na Lin

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Evaluation of genetic variants using chromosomal microarray analysis for fetuses with polyhydramnios by Xiaoqing Wu, Ying Li, Na Lin, Linjuan Su, Xiaorui Xie, Bing Liang, Qingmei Shen, Meiying Cai, Danhua Guo, Hailong Huang, Liangpu Xu

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Copy number variations (CNVs) and karyotyping analysis in males with azoospermia and oligospermia by Xing Xin, Peng Xu, Nan Wang, Yi Jiang, Jiaqiao Zhang, Shufang Li, Ying Zhu, Cong Zhang, Long Zhang, Hailong Huang, Ling Feng, Shaoshuai Wang

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