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FISH for Subtelomeric Region 20q
Advanced technology to detect subtle structural changes in chromosome 20q, aiding in early diagnosis of rare genetic disorders and ensuring a precise, well-informed clinical management plan for patients.
A specialized laboratory test using Fluorescence In Situ Hybridization (FISH) to evaluate the 20q subtelomeric region. It detects deletions or duplications linked to specific developmental or genetic syndromes.
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