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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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Detects mutations in genes associated with treatable neurometabolic disorders.
59,080 THB
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Detects mutations in genes related to metachromatic leukodystrophy, a lysosomal storage disease.
4,750 THB
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Detects genetic mutations associated with Prader-Willi and Angelman syndromes.
33,600 THB
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A two-step genetic test involving QF-PCR and karyotyping for prenatal diagnosis of chromosomal disorders.
12,075 THB
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Screens for carrier status of Spinal Muscular Atrophy and Fragile-X Syndrome.
23,310 THB
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Detects chromosomal abnormalities (trisomy 21) associated with Down syndrome.
8,505 THB
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Measures organic acids in urine, used to diagnose inborn errors of metabolism.
10,878 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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