Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
prenatal genetic test
|
| gptkbp:alternativeTo |
amniocentesis
chorionic villus sampling |
| gptkbp:detects |
gptkb:trisomy_21
trisomy 18 microdeletions sex chromosome aneuploidies trisomy 13 |
| gptkbp:developedBy |
gptkb:Sequenom
gptkb:Labcorp |
| https://www.w3.org/2000/01/rdf-schema#label |
MaterniT21 PLUS
|
| gptkbp:introducedIn |
2011
|
| gptkbp:marketedIn |
gptkb:United_States
|
| gptkbp:notDetects |
single gene disorders
|
| gptkbp:regulates |
laboratory-developed test
|
| gptkbp:targetAudience |
pregnant women at increased risk for fetal chromosomal abnormalities
|
| gptkbp:technology |
cell-free DNA analysis
|
| gptkbp:turnaroundTime |
about 1 week
|
| gptkbp:type |
maternal blood
|
| gptkbp:usedFor |
non-invasive prenatal testing
detection of fetal chromosomal abnormalities |
| gptkbp:bfsParent |
gptkb:Sequenom
|
| gptkbp:bfsLayer |
7
|