Search Results - "Yan, Huanchen"

Genetic Examination for Fetuses with Increased Fetal Nuchal Translucency by Genomic Technology by Xue, Shuya, Yan, Huanchen, Chen, Jingsi, Li, Nan, Wang, Jiayan, Liu, Yu, Zhang, Huimin, Li, Shaoying, Zhang, Wei, Chen, Dunjin, Chen, Min

“…This study aims to investigate the value of chromosomal microarray analysis (CMA) and whole exome sequencing (WES) in fetuses with increased nuchal…”
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Prenatal Diagnosis of Fetuses With Increased Nuchal Translucency by Genome Sequencing Analysis by Choy, Kwong Wai, Wang, Huilin, Shi, Mengmeng, Chen, Jingsi, Yang, Zhenjun, Zhang, Rui, Yan, Huanchen, Wang, Yanfang, Chen, Shaoyun, Chau, Matthew Hoi Kin, Cao, Ye, Chan, Olivia Y M, Kwok, Yvonne K, Zhu, Yuanfang, Chen, Min, Leung, Tak Yeung, Dong, Zirui

“…Increased nuchal translucency (NT) is an important biomarker associated with increased risk of fetal structural anomalies. It is known to be contributed by a…”
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The application of late amniocentesis: a retrospective study in a tertiary fetal medicine center in China by Li, Yingting, Yan, Huanchen, Chen, Jingsi, Chen, Fei, Jian, Wei, Wang, Jiayan, Ye, Xiaoqing, Li, Yufan, Li, Nan, Chiu, Philip C N, Chen, Min

“…To assess the indications and complications of late amniocentesis and the advanced genetic test results in a tertiary university fetal medical medicine unit…”
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Identification of copy number variants by NGS-based NIPT at low sequencing depth by Ye, Xiaoqing, Lin, Shengmou, Song, Xiwei, Tan, Meihua, Li, Jia, Wang, Jiayan, Yan, Huanchen, Zhang, Huimin, Li, Shaoying, Chen, Dunjin, Chen, Min

“…To explore the clinical utility of detecting chromosome copy number variants (CNVs) in the fetus by noninvasive prenatal testing (NIPT) using the low-pass…”
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Empowering Cartilage Restructuring with Biodegradable Magnesium Doped-Silicon Based-Nanoplatforms: Sustained Delivery and Enhanced Differentiation Potential by Chen, Min, Liu, Tao, Li, Wenqiang, Li, Yingting, Zhong, Puxin, Yan, Huanchen, Kong, Jingyin, Liang, Weixiang

“…Cartilage-related diseases, such as hypoplastic chondrodysplasia a rare genetic disorder that affects newborns, causing abnormal cartilage development and…”
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Validation of fetal DNA fraction estimation and its application in noninvasive prenatal testing for aneuploidy detection in multiple pregnancies by Chen, Min, Jiang, Fuman, Guo, Yulai, Yan, Huanchen, Wang, Jiayan, Zhang, Longmei, Zeng, XiaoJing, Li, Sheng, Li, Yufan, Li, Nan, Zhang, Chunsheng, Zhu, Wentao, Du, Bole, Wang, Yang, Lan, Zhiheng, Luo, Xingcheng, Luo, Fei, Chen, Dunjin

“…Objective To analyze the fetal fraction, fetal sex, and chromosomal aneuploidy in multiple pregnancies using noninvasive prenatal testing (NIPT). Method A…”
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Noninvasive prenatal sequencing for multiple Mendelian monogenic disorders among fetuses with skeletal dysplasia or increased nuchal translucency by Yan, Huanchen, Zhu, Xiaofan, Chen, Jingsi, Cao, Ye, Kwok, Yvonne Ka Yin, Chen, Zihan, Leung, Tak Yeung, Chen, Min, Choy, Kwong Wai

“…Objectives To evaluate the performance of noninvasive prenatal sequencing for multiple Mendelian monogenic disorders (NIPS‐M) among fetuses with skeletal…”
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