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Evidence for feasibility of fetal trophoblastic cell‐based noninvasive prenatal testing

116

Citations

39

References

2016

Year

Abstract

We believe that this is the first report of using array CGH and NGS whole genome sequencing to detect chromosomal abnormalities in fetal trophoblastic cells from maternal blood. © 2016 The Authors. Prenatal Diagnosis published by John Wiley & Sons, Ltd.

References

YearCitations

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