Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6143658 | American Journal of Obstetrics and Gynecology | 2016 | 30 Pages |
Abstract
This study has demonstrated that genomewide NIPT for fetal chromosomal abnormalities can provide high resolution, sensitive, and specific detection of a wide range of subchromosomal and whole chromosomal abnormalities that were previously only detectable by invasive karyotype analysis. In some instances, this NIPT also provided additional clarification about the origin of genetic material that had not been identified by invasive karyotype analysis.
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Authors
Roy B. PhD, John A. PhD, Tong PhD, Yijin PhD, Amin R. PhD, Eyad MS, Grant MS, Vach PhD, Chen PhD, Daniel S. MD, Graham MS, Mathias MD,