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FISH, Subtelomeric Regions (11p)
A specialized genetic test targeting the 11p subtelomeric region to detect copy-number abnormalities. This assay is crucial for identifying specific hereditary syndromes and ensuring accurate clinical diagnosis for patients.
An advanced laboratory test using Fluorescence In Situ Hybridization (FISH) to evaluate the 11p subtelomeric region. It detects microdeletions or duplications associated with developmental delays or congenital anomalies.
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