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Detects mutations in the alpha-globin gene, used in diagnosing alpha thalassemia.
10,500 THB
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Sequencing of the entire exome to identify genetic causes for undiagnosed conditions.
105,000 THB
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Detects mutations in the FGFR3 gene, associated with achondroplasia and other skeletal disorders.
7,245 THB
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Identifies mutations in the ACTA1 gene, associated with nemaline myopathy.
9,555 THB
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Detects the XmnI polymorphism in the HBG2 gene, which can influence the severity of beta-thalassemia.
7,176 THB
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