Automated genomic interpretation of sub-chromosomal fetal copy number variation by sequencing circulating cell-free DNA from maternal plasma

April 6, 2016
Previous Flipbook
Clinical experience of trisomy 16 and 22, and microdeletion detection by noninvasive prenatal testing (NIPT)
Clinical experience of trisomy 16 and 22, and microdeletion detection by noninvasive prenatal testing (NIPT)

Next Flipbook
Circulating cell-free DNA screening for fetal aneuploidy- the Newton-Wellesley Hospital Maternal Fetal Medicine experience
Circulating cell-free DNA screening for fetal aneuploidy- the Newton-Wellesley Hospital Maternal Fetal Medicine experience