Prenatal Diagnosis

<div>Traditional Prenatal Diagnosis: Past to Present.-&nbsp;Overview of Preimplantation Genetic Diagnosis (PGD): Historical Perspective and Future Direction.-&nbsp;Non-Invasive Approaches to Prenatal Diagnosis: Historical Perspective and Future Directions.-&nbsp;Molecular Testing for Preimplantation Genetic Diagnosis of Single Gene Disorders.-&nbsp;Detection of Aneuploidy and Unbalanced Rearrangements using Comparative Genomic Hybridization Microarrays.-&nbsp;Aneuploidy Screening using Next Generation Sequencing.-&nbsp;DNA Extraction from Various Types of Prenatal Specimens.-&nbsp;Assessment of Maternal Cell Contamination in Prenatal Samples by Quantitative Fluorescent PCR (QF-PCR).-&nbsp;Rapid Prenatal Aneuploidy Screening by Fluorescence In Situ Hybridization (FISH).-&nbsp;Prenatal Detection of Chromosome Aneuploidy by Quantitative Fluorescence PCR.-&nbsp;Multiplex Ligation-Dependent Probe Amplification (MLPA) for Prenatal Diagnosis of Common Aneuploidies.-&nbsp;Chromosomal Microarray Analysis using Array Comparative Genomic Hybridization on DNA from Amniotic Fluid and Chorionic Villus Sampling.- Prenatal Diagnosis using Chromosomal SNP Microarrays.-&nbsp;Rapid Detection of Fetal Mendelian Disorders: Thalassemia and Sickle Cell Syndromes.-&nbsp;Prenatal Diagnosis of Cystic Fibrosis.-&nbsp;Prenatal Diagnosis of Tay-Sachs Disease.-&nbsp;Next-Generation Sequencing of Prenatal Structural Chormosomal Rearrangements using Large-Insert Libraries.-&nbsp;Prenatal Diagnosis by Whole Exome Sequencing in Fetuses with Ultrasound Abnormalities.-&nbsp;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.-&nbsp;Isolation of Cell-Free DNA from Maternal Plasma.-&nbsp;Noninvasive Detection of Fetal Aneuploidy using Next-Generation Sequencing.-&nbsp;Noninvasive Antenatal Screening for Fetal RHD in RhD Negative Women to Guide Targeted Anti-D Prophylaxis.</div>