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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 mutations in the FGFR3 gene, associated with achondroplasia and other skeletal disorders.
7,245 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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Detects common alpha thalassemia mutations in prenatal specimens.
6,325 THB
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A two-step genetic test involving QF-PCR and karyotyping for prenatal diagnosis of chromosomal disorders.
12,075 THB
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Detects the presence of the SRY gene, used in determining male sex development.
4,000 THB
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