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Detects mutations in genes associated with types 6, 7, and 12 spinocerebellar ataxia.
10,427 THB
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Detects mutations in the ATXN7 gene, responsible for spinocerebellar ataxia type 7.
5,865 THB
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Detects mutations in the alpha-globin gene, used to diagnose alpha thalassemia.
4,375 THB
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Detects mutations in the beta-globin gene, used for diagnosing beta thalassemia.
7,015 THB
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Detects TSI antibodies to diagnose Graves’ disease, an autoimmune thyroid disorder.
26,928 THB
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Detects chromosomal deletions associated with DiGeorge syndrome, a genetic disorder.
8,505 THB
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Detects genetic mutations through whole exome sequencing, used in diagnosing rare genetic disorders.
78,750 THB
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Analyzes the exome of a patient and both parents (trio analysis) to detect genetic disorders.
143,500 THB
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Analyzes the whole genome of a proband and both parents to detect genetic variations and mutations.
217,880 THB
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