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Detects mutations in the alpha-globin gene, used in diagnosing alpha thalassemia.
10,500 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
Identifies mutations in the ACTA1 gene, associated with nemaline myopathy.
9,555 THB
Detects the XmnI polymorphism in the HBG2 gene, which can influence the severity of beta-thalassemia.
7,176 THB