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Detects chromosomal deletions associated with DiGeorge syndrome, a genetic disorder.
8,505 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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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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Detects microdeletions in the Y chromosome, which may cause male infertility.
29,250 THB
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