High resolution chromosome analysis is the method of choice in neonates for detecting numerical and structural chromosome aberrations. This assay not only detects extra chromosomes, such as chromosome 21 in Down syndrome, but it also identifies structural chromosome changes, including subtle deletions and additions not identified by conventional Karyotyping techniques.
Sample Type - Blood
Reporting Time - Please Call Customer care
Prerequisites - No special preparation required
Price - ₹4480/-
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