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LifeCell GenomeScope Newborn Screen for genetic disorders in healthy baby

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₹20,000.00
Short description:
A genomic test that detects inherited genetic conditions in newborns before any symptoms manifest. GenomeScope Newborn test identifies variations in genes associated with childhood-onset conditions before the appearance of any signs or symptoms. Insights from the test can enable timely...
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A genomic test that detects inherited genetic conditions in newborns before any symptoms manifest.
GenomeScope Newborn test identifies variations in genes associated with childhood-onset conditions before the appearance of any signs or symptoms. Insights from the test can enable timely intervention that paves the way for proactive health decisions as well as an informed future.

Sample Type : Umbilical Cord Blood or Heel prick
Collection Type : Paramedic
Results : Within 21 Days
Genes Tested : 1500

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