Most Recent Flipbooks
Expanding Noninvasive Prenatal Testing (NIPT) to Average Risk: MaterniT® 21 PLUS Performance in the Average Risk vs. High Risk Population
Abnormal ultrasound and increased yield of abnormal results with genome-wide cfDNA analysis
Expanding noninvasive prenatal testing (NIPT) for screening of unbalanced translocations
Genome wide detection of chromosomal gains and losses greater than 7Mb by cfDNA analysis
Clinical experience of trisomy 16 and 22, and microdeletion detection by noninvasive prenatal testing (NIPT)
Automated genomic interpretation of sub-chromosomal fetal copy number variation by sequencing circulating cell-free DNA from maternal plasma
Circulating cell-free DNA screening for fetal aneuploidy- the Newton-Wellesley Hospital Maternal Fetal Medicine experience
Identification of 22q11 microdeletions by noninvasive prenatal testing (NIPT) - the clinical experience
Karyotype-level noninvasive prenatal testing by sequencing of circulating cell-free DNA from maternal plasma
Noninvasive prenatal testing aids in detecting parental balanced translocation and highlights limitations of karyotyping
Rings and things- Noninvasive prenatal testing¹s unique view of the biology and embryology behind chromosomal ring formation and segregation
