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    Noninvasive Prenatal Testing (NIPT)

    Noninvasive Prenatal Testing (NIPT)

    - Applied Genomics in Prenatal Screening and Diagnosis

    Forfatter: info mangler
    Bog
    • Format
    • Bog, paperback
    • Engelsk

    Beskrivelse

    Since its introduction in 2012, cell-free (cf) DNA based Non-Invasive Prenatal Testing (NIPT) has been employed to test for fetal chromosome abnormalities, and gene mutations that lead to a variety of genetic conditions, by millions of pregnant women, in more than 90 countries worldwide. With Noninvasive Prenatal Testing (NIPT): Applied Genomics in Prenatal Screening and Diagnosis, Dr Lieve Page-Christiaens and Dr Hanns-Georg Klein have compiled the first authoritative volume on cfDNA NIPT methods and their clinical implementation.

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    Detaljer
    • SprogEngelsk
    • Sidetal405
    • Udgivelsesdato25-08-2018
    • ISBN139780128141892
    • Forlag Academic Press Inc
    • FormatPaperback
    Størrelse og vægt
  • Vægt840 g
    • coffee cup img
    10 cm
    book img
    19,1 cm
    23,5 cm

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    Screening Pregnancy History Ethics Gene therapy Genomics Informed Consent. Multiplexing Cost Quality assurance Standardization Down syndrome Down's syndrome Prenatal diagnosis Quality Accreditation Preeclampsia Placenta Cost-effectiveness Validation Sex chromosomes Patient safety Sex determination Plasma Twin Aneuploidy society Overview Health economics Tec Prenatal Testing Trophoblast Next generation sequencing Digital PCR Cancers Whole genome sequencing Immunoprophylaxis Wes Single Nucleotide Polymorphism Wgs RNA-Seq Exome sequencing Proficiency testing Copy number variation (CNV) Incidental findings Genetic Disease Stem cell therapy External quality assessment NGS Sex selection Mendelian Inheritance Prenatal screening Z-score Alloimmunization and correct if necessary.--> D Aneuploidy screening Cell-free fetal DNA Cell-based noninvasive prenatal testing Cell-free DNA-based noninvasive prenatal testing Cell-free DNA-based prenatal testing CfDNA cfDNA Screening cfDNA Testing Cell-free DNA NIPT Cell-free DNA prenatal testing Cell-free placental DNA Confined placental mosaicism (CPM) Cytogenomic External Quality Assessment Scheme Chorionicity copy number variants Decisional support De novo mutations cfDNA-based NIPT Fetal cells Fetal sexing Clinical exome Cluster generation Fetal neonatal alloimmune thrombocytopenia Confined Placental Mosaicism Fetal growth restriction Hemolytic disease of the fetus and newborn Fetal structural anomaly Human platelet antigens Economic Appraisal European Molecular Quality Network Microvesicle Fetal chromosomal aneuploidies Fetal fraction Fetal Therapy Maternal factor Maternal CNVs Fetal nucleated red blood cell Monogenic disorder NIPT implementation Noninvasive prenatal diagnosis Monogenic disorder detection Noninvasive fetal blood group typing Parent decision-making Prenatal genetic diagnosis Placental Abruption Informed choice Prenatal treatment Rare autosomal trisomies ISO 15189 selective abortion RhWould you consider changing the keyword Rh D to RhD? Please check Sex discordancy Test accuracy UK National External Quality Assessment Service Maternal mosaicism True fetal mosaicism Uniparental disomy (UPD) Vanishing twin Maternal malignancy NIPT Noninvasive prenatal testing sex chromosome aneuploidy PAGE Study Rare autosomal trisomy Sequencing by synthesis ultrasound scan reproductive autonomy Secondary findings Segmental aneuploidy Zygosity

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