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Carrier screening for common genetic conditions using next-generation sequencing and additional molecular methods.
35,840 THB
Detects genetic mutations through whole exome sequencing, used in diagnosing rare genetic disorders.
78,750 THB
Analyzes the exome of a patient and both parents (trio analysis) to detect genetic disorders.
143,500 THB
Whole genome sequencing to detect genetic mutations and variations across the entire genome.
103,500 THB
Analyzes the whole genome of a proband and both parents to detect genetic variations and mutations.
217,880 THB
Identifies mutations associated with Wilson disease, a genetic disorder affecting copper metabolism.
32,400 THB