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Detects alpha-thalassemia using amniotic fluid and parental blood samples, often during pregnancy.
5,500 THB
Detects chromosomal abnormalities through array CGH, useful for prenatal and postnatal diagnosis.
33,600 THB
Analyzes chromosomal abnormalities using fetal DNA, often performed on placental tissue or amniotic fluid.
73,920 THB
Detects mutations in the FGFR3 gene, associated with achondroplasia and other skeletal disorders.
7,245 THB
Detects genetic mutations associated with hereditary persistence of fetal hemoglobin.
9,713 THB
Detects alpha and beta thalassemia in a prenatal setting using sequencing of suspected alleles.
14,630 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 chromosomal abnormalities in fetuses, used in prenatal genetic diagnosis.
34,020 THB
Detects common alpha thalassemia mutations in prenatal specimens.
6,325 THB
A two-step genetic test involving QF-PCR and karyotyping for prenatal diagnosis of chromosomal disorders.
12,075 THB
Detects the presence of the SRY gene, used in determining male sex development.
4,000 THB