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Detects single nucleotide polymorphisms (SNPs) through pyrosequencing for various genetic conditions.

5,750 THB

Measures pyruvate kinase enzyme activity, used to diagnose pyruvate kinase deficiency, a cause of hemolytic anemia.

5,500 THB

A two-step genetic test involving QF-PCR and karyotyping for prenatal diagnosis of chromosomal disorders.

12,075 THB

A prenatal screening test to assess risk for Down syndrome, Edwards syndrome, and neural tube defects.

7,875 THB

A non-invasive prenatal test (NIPT) for detecting fetal chromosomal abnormalities using maternal blood.

31,500 THB

A premium non-invasive prenatal test that screens for chromosomal abnormalities and microdeletions.

34,020 THB

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

8,505 THB

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

16,739 THB

Detects mutations in the SCA6 gene, linked to spinocerebellar ataxia type 6.

6,900 THB

Detects mutations in genes associated with types 6, 7, and 12 spinocerebellar ataxia.

10,427 THB

Genetic sequencing test used for various conditions requiring sequence analysis.

7,015 THB

Screens for carrier status of Spinal Muscular Atrophy and Fragile-X Syndrome.

23,310 THB

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