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Preimplantation genetic testing for alpha thalassemia, using linked polymorphic markers to study familial alleles inheritance.
207,571 THB
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Preimplantation genetic testing for mutations in embryos using Sanger sequencing and STR analysis.
19,800 THB
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Identifies genetic mutations and inheritance patterns in embryos before implantation, used for families with a known risk of monogenic diseases.
365,781 THB
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Measures phosphofructokinase enzyme activity, used to diagnose glycogen storage diseases.
5,500 THB
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Detects mutations in PKD1 gene, used to diagnose autosomal dominant polycystic kidney disease (ADPKD).
44,800 THB
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Identifies mutations in alpha thalassemia through prenatal testing of amniotic fluid.
10,164 THB
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Detects beta-thalassemia in fetuses using amniotic fluid and parental blood samples.
6,440 THB
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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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