Prenatal Diagnosis 1st edition by Brynn Levy 1493988877 9781493988877

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ISBN 10: 1493988877 

ISBN 13: 9781493988877

Author: Brynn Levy 

This second edition volume expands on the first edition with more detailed methodologies on prenatal testing and diagnosis, and also covers next-generation sequencing techniques. The chapters in this book are divided into three sections: preimplantation genetic testing, traditional prenatal testing, and non-invasive prenatal testing. This book covers topics such as molecular testing for preimplantation genetic diagnosis of single gene disorders; DNA extraction from various types of prenatal specimens; prenatal diagnosis of cystic fibrosis and Tay-Sachs disease; chromosomal SNP microarrays; and isolation of cell-free DNA from maternal plasma. Written in the highly successful Methods in Molecular Biology series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls.

Prenatal Diagnosis 1st table of contents: 

1. Traditional Prenatal Diagnosis: Past to Present
2. Overview of Preimplantation Genetic Diagnosis (PGD): Historical Perspective and Future Direction
3. Noninvasive Approaches to Prenatal Diagnosis: Historical Perspective and Future Directions
4. Preimplantation Genetic Testing
5. Molecular Testing for Preimplantation Genetic Diagnosis of Single Gene Disorders
6. Detection of Aneuploidy and Unbalanced Rearrangements Using Comparative Genomic Hybridization Microarrays
7. Aneuploidy Screening using Next Generation Sequencing
8. Traditional Prenatal Diagnosis
9. DNA Extraction from Various Types of Prenatal Specimens
10. Assessment of Maternal Cell Contamination in Prenatal Samples by Quantitative Fluorescent PCR (QF-PCR)
11. Rapid Prenatal Aneuploidy Screening by Fluorescence In Situ Hybridization (FISH)
12. Prenatal Detection of Chromosome Aneuploidy by Quantitative Fluorescence PCR
13. Multiplex Ligation-Dependent Probe Amplification (MLPA) for Prenatal Diagnosis of Common Aneuploidies
14. Chromosomal Microarray Analysis Using Array Comparative Genomic Hybridization on DNA from Amniotic Fluid and Chorionic Villus Sampling
15. Prenatal Diagnosis Using Chromosomal SNP Microarrays
16. Rapid Detection of Fetal Mendelian Disorders: Thalassemia and Sickle Cell Syndromes
17. Prenatal Diagnosis of Cystic Fibrosis
18. Prenatal Diagnosis of Tay-Sachs Disease

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Tags: Prenatal, Diagnosis, Brynn Levy, expands, methodologies