top of page

Chromosomal Microarray

T009
EGP9,710.00
In stock
1
Product Details

Across the globe, chromosomal microarray (CMA) is quickly replacing traditional karyotyping as a first-tier genetic test to screen for suspected chromosomal anomalies, developmental disorders, epilepsy, hypotonia, multiple congenital anomalies, certain metabolic diseases, and other known conditions caused due to cytogenetic abnormalities.

  • The high-resolution, whole-genome technique helps detect the submicroscopic deletions/duplications called copy number variants (CNVs) in the chromosomes
  • CNVs are associated with a wide range of genetic disorders - Autism Spectrum disorders, autosomal disorders , X-linked Inheritance , UPD (Uniparental Disomy) and more.
Save this product for later

Accepted Payments:

Visa_2014_logo_detail.svg.png
Mastercard Logo.png
ACCEPT CMYK  LOGO - PNG.png
bottom of page