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Preimplantation genetic testing for alpha thalassemia, using linked polymorphic markers to study familial alleles inheritance.
207,571 THB
Preimplantation genetic testing for mutations in embryos using Sanger sequencing and STR analysis.
19,800 THB
Identifies genetic mutations and inheritance patterns in embryos before implantation, used for families with a known risk of monogenic diseases.
365,781 THB
Measures phosphofructokinase enzyme activity, used to diagnose glycogen storage diseases.
5,500 THB
Detects mutations in PKD1 gene, used to diagnose autosomal dominant polycystic kidney disease (ADPKD).
44,800 THB
Identifies mutations in alpha thalassemia through prenatal testing of amniotic fluid.
10,164 THB
Detects beta-thalassemia in fetuses using amniotic fluid and parental blood samples.
6,440 THB
Detects methylation abnormalities associated with Prader-Willi and Angelman syndromes using MS-MLPA.
12,236 THB
Detects chromosomal abnormalities in fetuses, used in prenatal genetic diagnosis.
34,020 THB
Detects common alpha thalassemia mutations in prenatal specimens.
6,325 THB
Detects mutations associated with primary torsion dystonia, a movement disorder.
3,458 THB