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Detects 5q chromosome deletion, used in diagnosing myelodysplastic syndromes.
10,500 THB
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Detects 16p13.3 deletions associated with Rubinstein-Taybi syndrome using FISH analysis.
9,188 THB
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Detects CGG-repeat expansions in the FMR1 gene, used to diagnose Fragile X syndrome.
11,400 THB
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Identifies mutations in the FXN gene, associated with Friedreich ataxia.
12,180 THB
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Screens for common G6PD mutations prevalent in Asian populations, associated with G6PD deficiency.
8,400 THB
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Detects mutations in the MEFV gene associated with Familial Mediterranean Fever (FMF), an inflammatory disorder.
12,075 THB
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Detects mutations in the HFE gene associated with hereditary hemochromatosis, a condition causing iron overload.
12,075 THB
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A customized genetic panel to analyze specific genes selected by the clinician.
67,200 THB
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