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Detects mutations in PKD1 gene, used to diagnose autosomal dominant polycystic kidney disease (ADPKD).
44,800 THB
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Detects beta-thalassemia in fetuses using amniotic fluid and parental blood samples.
6,440 THB
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Detects methylation abnormalities associated with Prader-Willi and Angelman syndromes using MS-MLPA.
12,236 THB
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Detects common alpha thalassemia mutations in prenatal specimens.
6,325 THB
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Detects mutations associated with primary torsion dystonia, a movement disorder.
3,458 THB
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Detects mutations in the protein C gene, used to diagnose protein C deficiency and related clotting disorders.
13,300 THB
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Detects mutations in genes associated with spinocerebellar ataxia types 1, 2, and 3.
8,505 THB
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Detects mutations in genes associated with spinocerebellar ataxia types 1, 2, and 3.
16,739 THB
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