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Detects mitochondrial DNA mutations associated with Leber hereditary optic neuropathy (LHON).
7,455 THB
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Detects mutations in mitochondrial DNA linked to MELAS, MERRF, and NARP syndromes.
7,245 THB
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Sequencing of the entire exome to identify genetic causes for undiagnosed conditions.
105,000 THB
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Screens for carriers of 130 genetic diseases using NGS.
71,680 THB
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Detects known family-specific variants, used for diagnosing inherited genetic disorders.
6,520 THB
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Detects mutations in the FGF23 gene, associated with phosphate regulation disorders.
13,300 THB
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Detects mutations in the FGFR2 gene, used to diagnose craniosynostosis syndromes like Apert syndrome.
7,245 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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