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Quantifies amino acids in urine for diagnosing aminoacidopathies. Includes 24 Items: Isoleucine, Leucine, Lysine, Methionine, Phenylalanine, Threonine, Tryptophan, Valine, Glycine, Serine, Taurine, Tyrosine, Asparagine, Aspartate, Cysteine, Alanine, Proli
38,000 THB
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Diagnoses the presence of fetal hemoglobin (HbF) in gastrointestinal bleeding in newborns using the APT test.
300 THB
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Assesses chromosomal abnormalities linked to developmental delays and autism spectrum disorder (ASD).
74,560 THB
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Detects mutations in the GJB2 gene, particularly exon 2, which are associated with congenital deafness.
7,770 THB
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A comprehensive screening for metabolic disorders, congenital hypothyroidism, and thalassemia in newborns.
11,550 THB
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Detects the genetic deletions or rearrangements associated with Alagille syndrome using FISH.
8,463 THB
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Detects 22q11 deletion associated with DiGeorge syndrome using FISH.
8,463 THB
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Detects 16p13.3 deletions associated with Rubinstein-Taybi syndrome using FISH analysis.
9,188 THB
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