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Detects methylation abnormalities associated with Prader-Willi and Angelman syndromes using MS-MLPA.
12,236 THB
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Detects chromosomal abnormalities in fetuses, used in prenatal genetic diagnosis.
34,020 THB
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Detects common alpha thalassemia mutations in prenatal specimens.
6,325 THB
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Detects mutations associated with primary torsion dystonia, a movement disorder.
3,458 THB
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Detects single nucleotide polymorphisms (SNPs) through pyrosequencing for various genetic conditions.
5,750 THB
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Measures pyruvate kinase enzyme activity, used to diagnose pyruvate kinase deficiency, a cause of hemolytic anemia.
5,500 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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A prenatal screening test to assess risk for Down syndrome, Edwards syndrome, and neural tube defects.
7,875 THB
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A non-invasive prenatal test (NIPT) for detecting fetal chromosomal abnormalities using maternal blood.
31,500 THB
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A premium non-invasive prenatal test that screens for chromosomal abnormalities and microdeletions.
34,020 THB
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Detects mutations in genes associated with spinocerebellar ataxia types 1, 2, and 3.
8,505 THB
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