Screening for common chromosomal changes plus specific microdeletion syndromes in the fetus.
Screening for the most common chromosomal changes plus specific microdeletion syndromes.
Generation Plus
Screening for specific chromosomal aneuploidies, as well as for specific sub-chromosomal imbalances (microdeletions) leading to known syndromes from 10 weeks onwards where there is a high risk of the known syndrome (e.g. a known previously affected pregnancy, or current pregnancy suspected of being affected based on ultrasound findings).
Chromosomes 13, 18, 21, X and Y plus 5 microdeletion syndromes
Whole Genome Sequencing (Illumina USA)
9 – 14 days from sample arriving at the laboratory
No
$799
Dedicated Generation NIPT request form required.
Blood
Streck Cell Free DNA BCT 10mL
Dedicated Generation NIPT request form available as a template in most practice management software.
This test is not available for testing of twin pregnancies. Testing is performed in our partner laboratory in California, USA.
Collection days are limited to Monday only.
