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Detects mutations in FGFR3 gene associated with thanatophoric dysplasia.
17,290 THB
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Detects chromosomal abnormalities (trisomy 21) associated with Down syndrome.
8,505 THB
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Detects chromosomal deletions associated with DiGeorge syndrome, a genetic disorder.
8,505 THB
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A non-invasive prenatal test using maternal blood to detect chromosomal abnormalities in the fetus.
39,600 THB
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Non-invasive prenatal test (NIPT) that screens for chromosomal abnormalities across all chromosomes.
42,000 THB
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Carrier screening for common genetic conditions using next-generation sequencing and additional molecular methods.
35,840 THB
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Detects genetic mutations through whole exome sequencing, used in diagnosing rare genetic disorders.
78,750 THB
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Analyzes the exome of a patient and both parents (trio analysis) to detect genetic disorders.
143,500 THB
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Whole genome sequencing to detect genetic mutations and variations across the entire genome.
103,500 THB
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Analyzes the whole genome of a proband and both parents to detect genetic variations and mutations.
217,880 THB
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Identifies mutations associated with Wilson disease, a genetic disorder affecting copper metabolism.
32,400 THB
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