Rapid Prenatal Testing for common aneuploidies
Trisomy 13 (Patau syndrome) Trisomy 18 (Edward syndrome) Trisomy 21 (Down syndrome) Triploidy Turner syndrome Klinefelter syndrome
PURPOSE OF PROGRAMME:
Analysis and interpretation of aneuploidy and fetal sexing prenatal samples: fixed cell suspensions for interphase FISH and/or DNA for QF-PCR studies.
MATERIAL PROVIDED: Cells: fixed suspension, DNA in TE buffer
DISTRIBUTIONS PER YEAR: 1
SAMPLES PER DISTRIBUTION: 5
FREQUENCY OF DISTRIBUTION: 1
PROGRAMME OF ANALYSIS:
Detection of common aneuploidies
Details of the performance criteria for this programme can be obtained from UK NEQAS Genomics (GenQA) directly.
Telephone: +44 (0) 131 2426898
From 1st January 2018, Cytogenomics External Quality Assessment Service (CEQAS) and UK National External Quality Assessment Service (UK NEQAS) for Molecular Genetics merged to become Genomics Quality Assessment (GenQA). Please click here for an overview of GenQA