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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

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

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