Prenatal diagnosis : edited by Brynn Levy.

Bibliographic Details
Other Authors:	Levy, Brynn (Editor)
Format:	Book
Language:	English
Published:	New York : Humana Press, [2019]
Edition:	Second edition.
Series:	Springer protocols (Series) Methods in molecular biology (Clifton, N.J.) ; v.1885.
Subjects:	Prenatal diagnosis. Fetus > Diseases > Molecular diagnosis. Prenatal Diagnosis. Fetal Diseases > diagnosis. Female. Pregnancy.

Table of Contents:

Traditional prenatal diagnosis : past to present
Overview of preimplantation genetic diagnosis (PGD) : historical perspective and future direction
Noninvasive approaches to prenatal diagnosis : historical perspective and future directions
Molecular testing for preimplantation genetic diagnosis of single gene disorders
Detection of aneuploidy and unbalanced rearrangements using comparative genomic hybridization microarrays
Aneuploidy screening using next generation sequencing - DNA extraction from various types of prenatal specimens
Assessment of maternal cell contamination in prenatal samples by quantitative fluorescent PCR (QF-PCR)
Rapid prenatal aneuploidy screening by fluorescence in situ hybridization (FISH)
Prenatal detection of chromosome aneuploidy by quantitative fluorescence PCR
Multiplex ligation-dependent probe amplification (MLPA) for prenatal diagnosis of common aneuploidies
Chromosomal microarray analysis using array comparative genomic hybridization on DNA from amniotic fluid and chorionic villus sampling
Prenatal diagnosis using chromosomal SNP microarrays
Rapid detection of fetal mendelian disorders : thalassemia and sickle cell syndromes
Prenatal diagnosis of cystic fibrosis
Prenatal diagnosis of Tay-Sachs disease
Next generation sequencing of prenatal structural chromosomal rearrangements using large-insert
Prenatal diagnosis by whole exome sequencing in fetuses with ultrasound abnormalities
Isolation and characterization of amniotic fluid-derived extracellular vesicles for biomarker discovery
Quad screen test, a multiplexed biomarker assay for prenatal screening to assess birth defects : the Columbia University experience using the Beckman Access2 immunoassay analyzer and Benetech PRA
Isolation of cell-free DNA from maternal plasma
Noninvasive detection of fetal aneuploidy using next generation sequencing
Noninvasive antenatal screening for fetal RHD in RhD negative women to guide targeted anti-D prophylaxis.