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Detects known family-specific variants, used for diagnosing inherited genetic disorders.
6,520 THB
Detects mutations in the FGFR2 gene, used to diagnose craniosynostosis syndromes like Apert syndrome.
7,245 THB
Detects mutations in the FGFR3 gene, associated with achondroplasia and other skeletal disorders.
7,245 THB
Detects 5q chromosome deletion, used in diagnosing myelodysplastic syndromes.
10,500 THB
Detects 16p13.3 deletions associated with Rubinstein-Taybi syndrome using FISH analysis.
9,188 THB
Detects CGG-repeat expansions in the FMR1 gene, used to diagnose Fragile X syndrome.
11,400 THB
Identifies mutations in the FXN gene, associated with Friedreich ataxia.
12,180 THB
Screens for common G6PD mutations prevalent in Asian populations, associated with G6PD deficiency.
8,400 THB
Detects mutations in the MEN1 gene, associated with multiple endocrine neoplasia type 1.
17,195 THB
Detects mutations in the MEFV gene associated with Familial Mediterranean Fever (FMF), an inflammatory disorder.
12,075 THB
A customized genetic panel to analyze specific genes selected by the clinician.
67,200 THB