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Detects mutations in the alpha-globin gene, used in diagnosing alpha thalassemia.
10,500 THB
Detects mutations associated with Crigler-Najjar syndrome, a rare genetic disorder affecting bilirubin metabolism.
11,875 THB
Sequencing of the entire exome to identify genetic causes for undiagnosed conditions.
105,000 THB
Detects mutations in the FGFR3 gene, associated with achondroplasia and other skeletal disorders.
7,245 THB
Screens for alpha and beta thalassemia and SMA carrier status using multiplex GAP-PCR and sequencing.
21,798 THB
Detects SNPs in ADIPOQ and LEPR genes associated with diabetes and overweight risk.
5,750 THB
Identifies mycobacterium species using sequencing, used in diagnosing tuberculosis and other mycobacterial infections.
8,820 THB
Identifies mutations in the ACTA1 gene, associated with nemaline myopathy.
9,555 THB
Detects known variants of abnormal hemoglobin using PCR and sequencing.
5,650 THB
Identifies mutations in alpha thalassemia through prenatal testing of amniotic fluid.
10,164 THB
Detects rotavirus and identifies specific viral types using PCR and sequencing.
11,875 THB