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Article

Identification of copy number variants by NGS-based NIPT at low sequencing depth

11 Nov 2020

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Share to Fetal and Pediatric Neurological Disorders
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 33310305
DOI: 10.1016/j.ejogrb.2020.11.026

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