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Lahalak Medical PlatformDifferentiate Care
FISH for Subtelomeric Region 22q
An advanced genetic screening to detect micro-chromosomal changes in chromosome 22, aiding in the assessment of genetic syndromes to ensure appropriate medical care and early intervention for your child.
A laboratory test using Fluorescence In Situ Hybridization (FISH) to examine chromosome 22 ends. It aims to detect deletions or duplications in genetic material linked to developmental syndromes.
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