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Comprehensive genetic cancer screening using next-generation sequencing (NGS).
107,100 THB
Analyzes the number and structure of chromosomes, often used to diagnose genetic abnormalities.
6,578 THB
Analyzes chromosomal abnormalities using fetal DNA, often performed on placental tissue or amniotic fluid.
73,920 THB
Detects mutations in genes associated with dentinogenesis imperfecta, a genetic disorder affecting tooth development.
5,865 THB
Analyzes genetic polymorphisms related to detoxification, used to assess detox capacity.
63,168 THB
Detects mitochondrial DNA mutations linked to Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia.
11,025 THB
Detects mitochondrial DNA mutations associated with Leber hereditary optic neuropathy (LHON).
7,455 THB
Detects mutations in mitochondrial DNA linked to MELAS, MERRF, and NARP syndromes.
7,245 THB
Sequencing of the entire exome to identify genetic causes for undiagnosed conditions.
105,000 THB
Measures Factor II (prothrombin) activity, used to diagnose blood clotting disorders.
7,350 THB
Detects the Factor II (prothrombin) mutation, which increases the risk of blood clots.
3,750 THB
Measures inhibitor levels against Factor VIII, used in managing hemophilia A patients.
8,820 THB