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  2. Non Invasive Prenatal Testing (NIPT) of trisomies 13, 18 et 21 and sex chromosomes

Non Invasive Prenatal Testing (NIPT) of trisomies 13, 18 et 21 and sex chromosomes

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Full name:
Non Invasive Prenatal Testing (NIPT) of trisomies 13, 18 et 21 and sex chromosomes
Test type:
Clinical
Test specialty:
Cytogenetics
Test purpose:
Prenatal diagnosis
Specimen:
Cell free DNA
Method category:
Detection of chromosome alteration large in size
Method technique:
Next Generation Sequencing (NGS)
Laboratory:
Centrum Menselijke Erfelijkheid - KUL
RIZIV code:
565611-565622
EQA:
  • 2015 NIPT for common aneuploidies Ringtest
  • 2016 NIPT for common aneuploidies Ringtest
  • 2017 NIPT for common aneuploidies GenQA (Genomics Quality Assessment)
  • 2018 NIPT for common aneuploidies GenQA (Genomics Quality Assessment)
  • 2019 NIPT for common aneuploidies GenQA (Genomics Quality Assessment)
  • 2020 NIPT for common aneuploidies GenQA (Genomics Quality Assessment)
  • 2021 NIPT for common aneuploidies GenQA (Genomics Quality Assessment)
  • 2022 NIPT for common aneuploidies GenQA (Genomics Quality Assessment)
Accreditation (ISO 15189):
2021-07-08 / 2026-02-02
Turnaround time (maximum):
7 calendar days
Document(s):
Created:
24 Jul 2019 - 09:55
Changed:
01 Mar 2023 - 15:58
URL:
https://laboboeken.nexuzhealth.com/pboek/internet/GHB%20CME/5464