Genetic counseling for a prenatal diagnosis of structural chromosomal abnormality with high-resolution analysis using a single nucleotide polymorphism microarray by Akiko Takashima, Naoki Takeshita, Toshihiko Kinoshita

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Application of Chromosomal Microarray Analysis in Genetic Reasons of Miscarriage Tissues by Xu Z, Liu N, Gao L, Yu D

Subjects: “…chromosomal microarray analysis…”
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Advances in chromosomal microarray analysis: Transforming neurology and neurosurgery by Wireko Andrew Awuah, Muhammad Hamza Shah, Vivek Sanker, Krishitha Meenu Mannan, Sruthi Ranganathan, Princess Afia Nkrumah-Boateng, Mabel Frimpong, Kwadwo Darko, Joecelyn Kirani Tan, Toufik Abdul-Rahman, Oday Atallah

Subjects: “…Chromosomal microarray analysis…”
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Clinical application of chromosomal microarray analysis for fetuses with craniofacial malformations by Chenyang Xu, Yanbao Xiang, Xueqin Xu, Lili Zhou, Huanzheng Li, Xueqin Dong, Shaohua Tang

Subjects: “…Chromosomal microarray analysis…”
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Clinical and genetic analysis of two phenotypically normal families carrying 4p16.1 microduplications by Xiaolin Wang, Yujiao Wang, Xinqiang Lan

Subjects: “…Chromosomal microarray analysis(CMA)…”
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Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype by Linjuan Su, Hailong Huang, Gang An, Meiying Cai, Xiaoqing Wu, Ying Li, Xiaorui Xie, Yuan Lin, Meiying Wang, Liangpu Xu

Subjects: “…chromosomal microarray analysis…”
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Chromosomal microarray analysis in fetuses with high-risk prenatal indications: A retrospective study in China by Xiaomei Luo, Hong Zhu, Lili Wang, Bing Xiao, Yanjie Fan, Hui Ye, Xiaomin Ying, Wenjuan Qiu, Huiwen Zhang, Lianshu Han, Xuefan Gu, Yongguo Yu, Lei Wang

Subjects: “…Chromosomal microarray analysis…”
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Diagnostic Value of Chromosomal Microarray Analysis for Fetal Congenital Heart Defects with Different Cardiac Phenotypes and Extracardiac Abnormalities by Simin Zhang, Jingjing Wang, Yan Pei, Jijing Han, Xiaowei Xiong, Yani Yan, Juan Zhang, Yan Liu, Fangfei Su, Jinyu Xu, Qingqing Wu

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Clinical utility of chromosomal microarray analysis and whole exome sequencing in foetuses with oligohydramnios by Xiaomei Shi, Hongke Ding, Chen Li, Ling Liu, LiHua Yu, Juan Zhu, Jing Wu

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Submicroscopic aberrations of chromosome 16 in prenatal diagnosis by Xiaoqing Wu, Liangpu Xu, Ying Li, Na Lin, Linjuan Su, Meiying Cai, Xiaorui Xie, Lin Zheng, Hailong Huang, Yuan Lin

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Prenatal diagnosis and genetic counseling of a paternally inherited chromosome 15q11.2 microdeletion in a Chinese family by Wenjuan Tang, Guowei Chen, Jingshu Xia, Ying Zhang

Subjects: “…Chromosomal microarray analysis (CMA)…”
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A Clinical and Molecular Description of a Rare Case of Chromosomal Abnormality (Partial Trisomy 14q11.2-q21.1 and Partial Monosomy 21q11.2-q21.3) by Grigory S. Vasilyev, Tatiana I. Meshcheryakova, Elena N. Lukash, Svetlana S. Zhylina, Ilya V. Kanivets, Alexander N. Petrin

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Analysis of genetic testing in fetuses with congenital heart disease of single atria and/or single ventricle in a Chinese prenatal cohort by Min Li, Baoying Ye, Yiyao Chen, Li Gao, Yi Wu, Weiwei Cheng

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Clinical value for the detection of fetal chromosomal deletions/duplications by noninvasive prenatal testing in clinical practice by Lingshan Gou, Feng Suo, Yi Wang, Na Wang, Qin Wu, Shunan Hu, Peng Wang, Lize Gu, Man Zhang, Chuanxia Wang, Yan Zhang, Xin Yin, Peng Zhang, Jian Xu, Xingqi Wang, Maosheng Gu

Subjects: “…chromosomal microarray analysis…”
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Application of chromosomal microarray analysis in products of miscarriage by Xiangyu Zhu, Jie Li, Yujie Zhu, Wanjun Wang, Xing Wu, Ying Yang, Leilei Gu, Yuanyuan Gu, Yali Hu

Subjects: “…Chromosomal microarray analysis…”
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Molecular and cytogenetic analysis of small supernumerary marker chromosomes in prenatal diagnosis by Yang Yang, Wang Hao

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Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysis by Ruibin Huang, Hang Zhou, Fang Fu, Ru Li, Tingying Lei, Yingsi Li, Ken Cheng, You Wang, Xin Yang, Lushan Li, Xiangyi Jing, Yongling Zhang, Fucheng Li, Dongzhi Li, Can Liao

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Case report: Cystic hygroma accompanied with campomelic dysplasia in the first trimester caused by haploinsufficiency with SOX9 deletion by Xijing Liu, Xijing Liu, Xijing Liu, Jianmin Wang, Jianmin Wang, Jianmin Wang, Mei Yang, Mei Yang, Mei Yang, Tian Tian, Tian Tian, Ting Hu, Ting Hu, Ting Hu

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Fetal congenital gastrointestinal obstruction: prenatal diagnosis of chromosome microarray analysis and pregnancy outcomes by Mengyao Ni, Xiangyu Zhu, Wei Liu, Leilei Gu, Yujie Zhu, Peixuan Cao, Yan Gu, Yan Xu, Chenyan Dai, Xing Wu, Ying Yang, Chunxiang Zhou, Jie Li

Subjects: “…Chromosomal microarray analysis…”
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Genetic Evaluation of 114 Chinese Short Stature Children in the Next Generation Era: a Single Center Study by Zhuo Huang, Yu Sun, Yanjie Fan, Lili Wang, Huili Liu, Zhuwen Gong, Jianguo Wang, Hui Yan, Yu Wang, Guorui Hu, Ruifang Wang, Jun Ye, Lianshu Han, Wenjuan Qiu, Huiwen Zhang, Lili Liang, Yu Yang, Andrew Dauber, Yongguo Yu, Xue-Fan Gu

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