Filter By Categories

All Categories filter

Diseases Category

Symptoms Category

Lifestyle Category

Age Groups Category

Category by Diagnostic Methods

Category by Specimen

Detects mutations in PKD1 gene, used to diagnose autosomal dominant polycystic kidney disease (ADPKD).

44,800 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 mutations in the protein C gene, used to diagnose protein C deficiency and related clotting disorders.

13,300 THB

Detects mutations in genes associated with spinocerebellar ataxia types 1, 2, and 3.

8,505 THB

เธ•เธฐเธเธฃเน‰เธฒเธชเธดเธ™เธ„เน‰เธฒ
Scroll to Top