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Lahalak Medical PlatformDifferentiate Care
Fluorescence In Situ Hybridization (FISH) for 16p Subtelomeric Region
Detect subtle genetic changes in the 16p chromosome using advanced FISH technology, aiding in the diagnosis of genetic syndromes and developmental delays with high precision for your family's health.
A specialized laboratory test using fluorescent probes to detect deletions or rearrangements in the 16p subtelomeric regions, essential for diagnosing complex genetic disorders.
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