- Chromosomal Microarray (CMA-315K) (1)
- Chromosomal Microarray (CMA-315K)
- DNA Storage (1)
- DNA Storage
- QF-PCR- 13, 18, 21, X & Y (1)
- QF-PCR- 13, 18, 21, X & Y
Comprehensive Prenatal Genetic Testing: QF-PCR and Chromosomal Microarray (CMA)
Our Comprehensive Prenatal Genetic Testing package combines two advanced genetic tests, QF-PCR (Basic) and Chromosomal Microarray (CMA-315K), to provide you with a thorough assessment of your baby’s genetic health during pregnancy. Additionally, the package includes DNA storage, ensuring the safekeeping of your baby’s genetic information for future reference.
QF-PCR – 13, 18, 21, X & Y: QF-PCR is a rapid and reliable test that analyzes specific regions of chromosomes 13, 18, 21, X, and Y. This test helps detect common chromosomal abnormalities, such as trisomy 21 (Down syndrome), trisomy 18 (Edwards syndrome), and trisomy 13 (Patau syndrome), as well as sex chromosome anomalies.
Chromosomal Microarray (CMA-315K): Chromosomal Microarray is a high-resolution genetic test that examines the fetal DNA for small genetic changes, including microdeletions and microduplications. CMA can identify a broader range of genetic disorders, providing more detailed and comprehensive information compared to traditional testing methods.
DNA Storage: Preserving your baby’s DNA offers peace of mind and serves as a valuable resource for future medical investigations. DNA storage ensures that your baby’s genetic information is securely stored, allowing you to access it if needed for potential genetic analyses later in life.
With our Comprehensive Prenatal Genetic Testing package, you can gain valuable insights into your baby’s genetic well-being, enabling informed decision-making and appropriate medical care during your pregnancy journey.