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Comprehensive metabolic panel for newborns to detect inborn errors of metabolism.
10,500 THB
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Detects 16p13.3 deletions associated with Rubinstein-Taybi syndrome using FISH analysis.
9,188 THB
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Detects CGG-repeat expansions in the FMR1 gene, used to diagnose Fragile X syndrome.
11,400 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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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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