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Detects mutations and deletions in the beta-globin (HBB) gene, used to diagnose beta-thalassemia and other hemoglobinopathies.
10,710 THB
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Detects mutations in the UGT1A1 gene, which cause Crigler-Najjar syndrome, a disorder that affects bilirubin metabolism.
11,875 THB
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Detects mutations in the CSF3R gene, which are linked to various blood disorders, including chronic neutrophilic leukemia.
9,723 THB
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Detects mutations in the HFE gene, which can cause hereditary hemochromatosis, leading to excessive iron absorption.
11,550 THB
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Detects mutations in the IDH1 and IDH2 genes, commonly found in leukemia and brain tumors.
12,350 THB
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Detects mutations in exon 2, 3, and 4 of the MECP2 gene, associated with Rett syndrome, a neurodevelopmental disorder primarily affecting females.
15,390 THB
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