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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
Diagnoses the presence of fetal hemoglobin (HbF) in gastrointestinal bleeding in newborns using the APT test.
300 THB
Assesses chromosomal abnormalities linked to developmental delays and autism spectrum disorder (ASD).
74,560 THB
Detects mutations in the GJB2 gene, particularly exon 2, which are associated with congenital deafness.
7,770 THB
A comprehensive screening for metabolic disorders, congenital hypothyroidism, and thalassemia in newborns.
11,550 THB
Detects the genetic deletions or rearrangements associated with Alagille syndrome using FISH.
8,463 THB
Detects 22q11 deletion associated with DiGeorge syndrome using FISH.
8,463 THB
Detects 16p13.3 deletions associated with Rubinstein-Taybi syndrome using FISH analysis.
9,188 THB
A comprehensive newborn metabolic disorder screening test using tandem mass spectrometry.
10,290 THB
Newborn screening for thalassemia using capillary electrophoresis to detect abnormal hemoglobin.
6,440 THB
Detects deletions or uniparental disomy associated with Prader-Willi syndrome using FISH.
8,820 THB
Detects methylation abnormalities associated with Prader-Willi and Angelman syndromes using MS-MLPA.
12,236 THB