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Added value of chromosomal microarray analysis over conventional karyotyping in stillbirth work‐up: systematic review and meta‐analysis
Martinez‐Portilla, R. J., Pauta, M., Hawkins‐Villarreal, A., Rial‐Crestelo, M., Paz y Miño, F., Madrigal, I., Figueras, F., Borrell, A.
Published in Ultrasound in obstetrics & gynecology (01.05.2019)
Published in Ultrasound in obstetrics & gynecology (01.05.2019)
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Prenatal diagnosis and molecular cytogenetic characterization of fetuses with central nervous system anomalies using chromosomal microarray analysis: a seven-year single-center retrospective study
Zhuang, Jianlong, Zhang, Na, Chen, Yu’e, Jiang, Yuying, Chen, Xinying, Chen, Wenli, Chen, Chunnuan
Published in Scientific reports (27.01.2024)
Published in Scientific reports (27.01.2024)
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Prenatal diagnosis and genetic etiology analysis of talipes equinovarus by chromosomal microarray analysis
Xie, Xiaorui, Huang, Baojia, Su, Linjuan, Cai, Meiying, Chen, Yuqin, Wu, Xiaoqing, Xu, Liangpu
Published in BMC medical genomics (20.11.2023)
Published in BMC medical genomics (20.11.2023)
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Prenatal diagnosis of fetuses conceived by assisted reproductive technology by karyotyping and chromosomal microarray analysis
Guo, Huan, Sheng, Rui, Zhang, Xiu, Jin, Xuemei, Gu, Wenjing, Liu, Ting, Dong, Haixin, Jia, Ran
Published in PeerJ (San Francisco, CA) (17.01.2023)
Published in PeerJ (San Francisco, CA) (17.01.2023)
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Clinical application of chromosomal microarray analysis for the prenatal diagnosis of chromosomal abnormalities and copy number variations in fetuses with congenital heart disease
Xia, Yu, Yang, Yongchao, Huang, Shufang, Wu, Yueheng, Li, Ping, Zhuang, Jian
Published in Prenatal diagnosis (01.05.2018)
Published in Prenatal diagnosis (01.05.2018)
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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 experience
Wu, Xiaoqing, He, Shuqiong, Li, Ying, Guo, Danhua, Chen, Xuemei, Liang, Bin, Wang, Meiying, Huang, Hailong, Xu, Liangpu
Published in BMC pregnancy and childbirth (26.01.2023)
Published in BMC pregnancy and childbirth (26.01.2023)
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The Genetic Etiology Diagnosis of Fetal Growth Restriction Using Single-Nucleotide Polymorphism-Based Chromosomal Microarray Analysis
Chen, Yu'e, Xie, Yingjun, Jiang, Yuying, Luo, Qi, Shi, Lijing, Zeng, Shuhong, Zhuang, Jianlong, Lyu, Guorong
Published in Frontiers in pediatrics (15.10.2021)
Published in Frontiers in pediatrics (15.10.2021)
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Identification of a novel isolated 4q35.2 microdeletion in a Chinese pediatric patient using chromosomal microarray analysis: a case report and literature review
Zhuang, Jianlong, Liu, Shufen, Chen, Xinying, Jiang, Yuying, Chen, Chunnuan
Published in Molecular cytogenetics (02.08.2023)
Published in Molecular cytogenetics (02.08.2023)
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Chromosomal microarray analysis of 410 Han Chinese patients with autism spectrum disorder or unexplained intellectual disability and developmental delay
Liu, Yi, Lv, Yuqiang, Zarrei, Mehdi, Dong, Rui, Yang, Xiaomeng, Higginbotham, Edward J., Li, Yue, Zhao, Dongmei, Song, Fengling, Yang, Yali, Zhang, Haiyan, Wang, Ying, Scherer, Stephen W., Gai, Zhongtao
Published in Npj genomic medicine (12.01.2022)
Published in Npj genomic medicine (12.01.2022)
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Chromosomal Aneuploidy Associated With Clinical Characteristics of Pregnancy Loss
Gu, Chongjuan, Li, Kuanrong, Li, Ru, Li, Ling, Li, Xiaojun, Dai, Xinyu, He, Yaojuan
Published in Frontiers in genetics (15.04.2021)
Published in Frontiers in genetics (15.04.2021)
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Genetic etiology and pregnancy outcomes of fetal hyperechoic kidneys: a retrospective analysis
Cai, Meiying, Lin, Na, Xiao, Ziheng, Huang, Hailong, Zheng, Lin, Xu, Liangpu
Published in Frontiers in pediatrics (20.08.2025)
Published in Frontiers in pediatrics (20.08.2025)
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Increased TBX6 gene dosages induce congenital cervical vertebral malformations in humans and mice
Ren, Xiaojun, Yang, Nan, Wu, Nan, Xu, Ximing, Chen, Weisheng, Zhang, Ling, Li, Yingping, Du, Ren-Qian, Dong, Shuangshuang, Zhao, Sen, Chen, Shuxia, Jiang, Li-Ping, Wang, Lianlei, Zhang, Jianguo, Wu, Zhihong, Jin, Li, Qiu, Guixing, Lupski, James R, Shi, Jiangang, Zhang, Feng, Liu, Pengfei
Published in Journal of medical genetics (01.06.2020)
Published in Journal of medical genetics (01.06.2020)
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Prenatal Diagnosis of Chromosomal Mosaicism in 18,369 Cases of Amniocentesis
Kang, Han, Wang, Lingxi, Xie, Yamei, Chen, Yifei, Gao, Chonglan, Li, Xingyu, Hu, Yu, Liu, Qingsong
Published in American journal of perinatology (01.05.2024)
Published in American journal of perinatology (01.05.2024)
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Characterization of Associated Nonclassical Phenotypes in Patients with Deletion in the WAGR Region Identified by Chromosomal Microarray: New Insights and Literature Review
de Souza, Vanessa Sodré, da Cunha, Gabriela Corassa Rodrigues, Versiani, Beatriz R., de Oliveira, Claudiner Pereira, Rosa, Maria Teresa Alves Silva, de Oliveira, Silviene F., Moretti, Patricia N., Mazzeu, Juliana F., Pic-Taylor, Aline
Published in Molecular syndromology (01.07.2022)
Published in Molecular syndromology (01.07.2022)
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Genomic imbalance in euploid pregnancy loss
Gu, Chongjuan, Li, Kuanrong, Li, Ling, Gao, Huan, Li, Ru, He, Yaojuan
Published in Journal of assisted reproduction and genetics (01.09.2022)
Published in Journal of assisted reproduction and genetics (01.09.2022)
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Molecular cytogenetic characterization of isolated recurrent 4q35.2 microduplication in Chinese population: a seven-year single-center retrospective study
Zhuang, Jianlong, Wei, Qiulan, Jiang, Yuying, Zeng, Shuhong, Lou, Haijuan, Zhang, Na, Chen, Chunnuan
Published in BMC pregnancy and childbirth (18.09.2024)
Published in BMC pregnancy and childbirth (18.09.2024)
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