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Detects known family-specific variants, used for diagnosing inherited genetic disorders.
6,520 THB
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Detects FGFR1 gene rearrangements, often linked to cancers like myeloproliferative disorders.
118,680 THB
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Detects mutations in the FGF23 gene, associated with phosphate regulation disorders.
13,300 THB
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Detects mutations in the FGFR2 gene, used to diagnose craniosynostosis syndromes like Apert syndrome.
7,245 THB
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Detects mutations in the FGFR3 gene, associated with achondroplasia and other skeletal disorders.
7,245 THB
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Detects FIP1L1-PDGFRA fusion gene associated with myeloid neoplasms, particularly eosinophilic leukemia.
7,056 THB
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Screens for chromosomal abnormalities (Down syndrome) during the first trimester of pregnancy.
4,075 THB
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