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Fluorescence In Situ Hybridization (FISH) for Subtelomeric Region 17p
A precise genetic test using FISH technology to detect micro-structural changes in the 17p subtelomeric region, aiding in the accurate diagnosis of rare genetic syndromes.
A specialized lab test identifying deletions or duplications at the 17p chromosome end. It aids in diagnosing Miller-Dieker syndrome or unexplained developmental disorders.
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