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Detects the HbH (Hemoglobin H) disease-causing gene, an alpha-thalassemia variant.
3,750 THB
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Comprehensive genetic panel for detecting mutations linked to hereditary hearing loss.
107,100 THB
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Detects the INT22 inversion mutation in Hemophilia A patients.
5,865 THB
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Detects genetic mutations associated with hereditary persistence of fetal hemoglobin.
9,713 THB
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Detects expansion mutations in the HTT gene, used to diagnose Huntingtonโs disease.
7,770 THB
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Detects mutations in the immunoglobulin heavy chain variable region (IGHV), used in diagnosing chronic lymphocytic leukemia (CLL).
34,000 THB
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Identifies and classifies leukemia cells based on surface markers, aiding in diagnosis and treatment planning.
17,575 THB
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