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Comprehensive screening for thalassemia using PCR methods to identify mutations in alpha and beta thalassemia.
14,630 THB
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Detects mutations associated with Crigler-Najjar syndrome, a rare genetic disorder affecting bilirubin metabolism.
11,875 THB
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Detects mutations in the SRD5A2 gene, used to diagnose 5-alpha reductase deficiency.
17,908 THB
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Analyzes beta-globin gene mutations for diagnosing hemoglobinopathies.
9,240 THB
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Detects mitochondrial DNA mutations linked to Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia.
11,025 THB
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Detects mitochondrial DNA mutations associated with Leber hereditary optic neuropathy (LHON).
7,455 THB
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Detects mutations in mitochondrial DNA linked to MELAS, MERRF, and NARP syndromes.
7,245 THB
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Detects Entamoeba histolytica DNA, used to diagnose amoebic dysentery or liver abscess.
6,900 THB
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