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Screens for multiple genetic mutations associated with hereditary colorectal cancer using next-generation sequencing (NGS).
107,100 THB
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Identifies mutations in the GJB1 gene associated with hereditary hearing loss.
17,338 THB
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Screens for carrier status of 62 genetic disorders including thalassemia, SMA, and FMR1.
35,416 THB
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Comprehensive genetic carrier screening for multiple inherited conditions, designed for preconception and early pregnancy planning.
35,416 THB
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Detects the HLA-B*1502 allele, used to assess risk for severe drug reactions, particularly Stevens-Johnson syndrome, in response to certain medications.
17,480 THB
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Detects mutations in the immunoglobulin heavy chain variable region (IGHV), used in diagnosing chronic lymphocytic leukemia (CLL).
34,000 THB
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Genetic testing for mutations associated with amyotrophic lateral sclerosis (ALS).
59,080 THB
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Genetic testing for hereditary aortic disorders, including Marfan syndrome and other aortopathies.
59,080 THB
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