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Boosted exome sequencing for diagnosing genetic conditions, focusing on the proband (the affected individual).

120,690 THB

Whole-exome sequencing of three family members (proband and both parents) to diagnose genetic disorders.

198,497 THB

Detects deletions or uniparental disomy associated with Prader-Willi syndrome using FISH.

8,820 THB

Detects genetic mutations through whole exome sequencing, used in diagnosing rare genetic disorders.

78,750 THB

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