Yaoshen Wang
6PUBLICATIONS
4CO-AUTHORS
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Publications (6)
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|Apr 03, 2021
Whole Genome Sequencing in the Evaluation of Fetal Structural Anomalies: A Parallel Test with Chromosomal Microarray Plus Whole Exome Sequencing.Jia Zhou, Ziying Yang, Jun Sun
|Sep 05, 2020
NGS-based spinal muscular atrophy carrier screening of 10,585 diverse couples in China: a pan-ethnic study.Sumin Zhao, Wanyang Wang, Yaoshen Wang
|Jan 10, 2020
Noninvasive prenatal diagnosis for Duchenne muscular dystrophy based on the direct haplotype phasing.Min Chen, Chao Chen, Xiaoyan Huang
|Oct 03, 2018
Pilot study of expanded carrier screening for 11 recessive diseases in China: results from 10,476 ethnically diverse couples.Sumin Zhao, Jiale Xiang, Chunna Fan
|Jan 11, 2018
Haplotype-based Noninvasive Prenatal Diagnosis of Hyperphenylalaninemia through Targeted Sequencing of Maternal Plasma.Jun Ye, Chao Chen, Yuan Yuan
|Aug 09, 2017
Noninvasive prenatal diagnosis of 21-Hydroxylase deficiency using target capture sequencing of maternal plasma DNA.Dingyuan Ma, Yuan Yuan, Chunyu Luo
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