Home » Genetic Disorders » صفحة 13
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Detects mutations in genes associated with spinocerebellar ataxia types 1, 2, and 3.
16,739 THB
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Detects mutations in genes associated with types 6, 7, and 12 spinocerebellar ataxia.
10,427 THB
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Genetic sequencing test used for various conditions requiring sequence analysis.
7,015 THB
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Screens for carrier status of Spinal Muscular Atrophy and Fragile-X Syndrome.
23,310 THB
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Screens for genetic variations associated with various health conditions, disease risks, and lifestyle factors using SNP array and polygenic risk scoring.
43,600 THB
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Detects the presence of the SRY gene, used in determining male sex development.
4,000 THB
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