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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 genetic mutations associated with hereditary persistence of fetal hemoglobin.
9,713 THB
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Detects expansion mutations in the HTT gene, used to diagnose Huntington’s disease.
7,770 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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Boosted exome sequencing for diagnosing genetic conditions, focusing on the proband (the affected individual).
120,690 THB
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Whole-exome sequencing of three family members (proband and both parents) to diagnose genetic disorders.
198,497 THB
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Genetic testing for hereditary connective tissue disorders, such as Ehlers-Danlos syndrome.
46,304 THB
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Detects mutations in the CFTR gene, associated with cystic fibrosis.
46,304 THB
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A broad genetic health screen analyzing exome sequences for various health conditions.
49,760 THB
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Detects mutations associated with inherited retinal diseases, including retinitis pigmentosa.
46,304 THB
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Detects mutations in NF1 and NF2 genes associated with neurofibromatosis types 1 and 2.
34,736 THB
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