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Detects alpha-thalassemia using amniotic fluid and parental blood samples, often during pregnancy.

5,500 THB

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Detects chromosomal abnormalities through array CGH, useful for prenatal and postnatal diagnosis.

33,600 THB

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Analyzes chromosomal abnormalities using fetal DNA, often performed on placental tissue or amniotic fluid.

73,920 THB

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Detects genetic mutations associated with hereditary persistence of fetal hemoglobin.

9,713 THB

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Detects alpha and beta thalassemia in a prenatal setting using sequencing of suspected alleles.

14,630 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 chromosomal abnormalities in fetuses, used in prenatal genetic diagnosis.

34,020 THB

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