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Microscopic examination of body fluids or swabs for the presence of pathogens, used to diagnose infections.
250 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
Detects the XmnI polymorphism in the HBG2 gene, which can influence the severity of beta-thalassemia.
7,176 THB
Determines zygosity for Hb CS-PS mutations using direct sequencing.
5,000 THB