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Prenatal Diagnosis

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Cover of 'Prenatal Diagnosis'

Table of Contents

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    Book Overview
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    Chapter 1 Spectral Karyotyping (SKY): Applications in Prenatal Diagnostics
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    Chapter 2 Characterization of Prenatally Assessed De Novo Small Supernumerary Marker Chromosomes by Molecular Cytogenetics
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    Chapter 3 Rapid Prenatal Aneuploidy Screening by Fluorescence In Situ Hybridization (FISH)
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    Chapter 4 Application of Multi-PRINS to Simultaneously Identify Chromosomes 18, X, and Y in Prenatal Diagnosis
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    Chapter 5 Prenatal Diagnosis Using Array CGH
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    Chapter 6 Prenatal Detection of Chromosome Aneuploidy by Quantitative Fluorescence PCR
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    Chapter 7 Real-Time Quantitative PCR for the Detection of Fetal Aneuploidies
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    Chapter 8 MLPA for Prenatal Diagnosis of Commonly Occurring Aneuploidies
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    Chapter 9 MALDI-TOF Mass Spectrometry for Trisomy Detection
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    Chapter 10 Rapid Detection of Fetal Mendelian Disorders: Thalassemia and Sickle Cell Syndromes
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    Chapter 11 Rapid detection of fetal Mendelian disorders: Tay-Sachs disease.
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    Chapter 12 Arrayed Primer Extension Reaction for Genotyping on Oligonucleotide Microarray
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    Chapter 13 A Fast Microelectronic Array for Screening and Prenatal Diagnosis of β-Thalassemia
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    Chapter 14 RHD Genotyping from Maternal Plasma: Guidelines and Technical Challenges
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    Chapter 15 Isolation of Cell-Free DNA from Maternal Plasma Using Manual and Automated Systems
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    Chapter 16 Fetal DNA: Strategies for Optimal Recovery
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    Chapter 17 Quantification of Circulatory Fetal DNA in the Plasma of Pregnant Women
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    Chapter 18 Detection and Quantification of Fetal DNA in Maternal Plasma by Using LightCycler Technology
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    Chapter 19 Size Fractionation of Cell-Free DNA in Maternal Plasma and Its Application in Noninvasive Detection of Fetal Single Gene Point Mutations
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    Chapter 20 MALDI-TOF Mass Spectrometry for Analyzing Cell-Free Fetal DNA in Maternal Plasma
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    Chapter 21 Isolation of Cell-Free RNA from Maternal Plasma
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    Chapter 22 A Microarray Approach for Systematic Identification of Placental-Derived RNA Markers in Maternal Plasma
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    Chapter 23 A Novel Method to Identify Syncytiotrophoblast-Derived RNA Products Representative of Trisomy 21 Placental RNA in Maternal Plasma
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    Chapter 24 Method for Extraction of High-Quantity and -Quality Cell-Free DNA from Amniotic Fluid
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    Chapter 25 Detection of New Screening Markers for Fetal Aneuploidies in Maternal Plasma: A Proteomic Approach
Attention for Chapter 2: Characterization of Prenatally Assessed De Novo Small Supernumerary Marker Chromosomes by Molecular Cytogenetics
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Chapter title
Characterization of Prenatally Assessed De Novo Small Supernumerary Marker Chromosomes by Molecular Cytogenetics
Chapter number 2
Book title
Prenatal Diagnosis
Published in
Methods in molecular biology, January 2008
DOI 10.1007/978-1-59745-066-9_2
Pubmed ID
Book ISBNs
978-1-58829-803-4, 978-1-59745-066-9

Thomas Liehr