Noninvasive prenatal testing for fetal subchromosomal copy number variations and chromosomal aneuploidy by low‐pass whole‐genome sequencing
- DOI
- 10.1002/mgg3.674
- Published
- 2019-04-19
- Container
- Molecular Genetics & Genomic Medicine
- Publisher
- Wiley
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1002/mgg3.674,
title = {Noninvasive prenatal testing for fetal subchromosomal copy number variations and chromosomal aneuploidy by low‐pass whole‐genome sequencing},
author = {Dongyi Yu and Kai Zhang and Meiyan Han and Wei Pan and Ying Chen and Yunfeng Wang and Hongyan Jiao and Ling Duan and Qiying Zhu and Xiaojie Song and Yan Hong and Chen Chen and Juan Wang and Feng Hui and Linzhou Huang and Chongjian Chen and Yang Du},
year = {2019},
journal = {Molecular Genetics \& Genomic Medicine},
doi = {10.1002/mgg3.674},
url = {https://doi.org/10.1002/mgg3.674}
}RIS
TY - JOUR TI - Noninvasive prenatal testing for fetal subchromosomal copy number variations and chromosomal aneuploidy by low‐pass whole‐genome sequencing AU - Dongyi Yu AU - Kai Zhang AU - Meiyan Han AU - Wei Pan AU - Ying Chen AU - Yunfeng Wang AU - Hongyan Jiao AU - Ling Duan AU - Qiying Zhu AU - Xiaojie Song AU - Yan Hong AU - Chen Chen AU - Juan Wang AU - Feng Hui AU - Linzhou Huang AU - Chongjian Chen AU - Yang Du PY - 2019 JO - Molecular Genetics & Genomic Medicine DO - 10.1002/mgg3.674 UR - https://doi.org/10.1002/mgg3.674 ER -
APA
Yu, D., Zhang, K., Han, M., Pan, W., Chen, Y., Wang, Y., Jiao, H., Duan, L., Zhu, Q., Song, X., Hong, Y., Chen, C., Wang, J., Hui, F., Huang, L., Chen, C., & Du, Y. (2019). Noninvasive prenatal testing for fetal subchromosomal copy number variations and chromosomal aneuploidy by low‐pass whole‐genome sequencing. Molecular Genetics & Genomic Medicine. https://doi.org/10.1002/mgg3.674
Source records
- crossref · retrieved 2026-09-26T05:00:13.414Z