Filter By Categories
All Categories filter
Diseases Category
Symptoms Category
Lifestyle Category
Age Groups Category
Category by Diagnostic Methods
Category by Specimen
Detects alpha-thalassemia using amniotic fluid and parental blood samples, often during pregnancy.
5,500 THB
Add to WishlistRemove from Wishlist
Add to Wishlist
Detects chromosomal abnormalities through array CGH, useful for prenatal and postnatal diagnosis.
33,600 THB
Add to WishlistRemove from Wishlist
Add to Wishlist
Analyzes chromosomal abnormalities using fetal DNA, often performed on placental tissue or amniotic fluid.
73,920 THB
Add to WishlistRemove from Wishlist
Add to Wishlist
Detects mutations in the FGFR3 gene, associated with achondroplasia and other skeletal disorders.
7,245 THB
Add to WishlistRemove from Wishlist
Add to Wishlist
Detects genetic mutations associated with hereditary persistence of fetal hemoglobin.
9,713 THB
Add to WishlistRemove from Wishlist
Add to Wishlist
Detects alpha and beta thalassemia in a prenatal setting using sequencing of suspected alleles.
14,630 THB
Add to WishlistRemove from Wishlist
Add to Wishlist
Identifies mutations in alpha thalassemia through prenatal testing of amniotic fluid.
10,164 THB
Add to WishlistRemove from Wishlist
Add to Wishlist
Detects beta-thalassemia in fetuses using amniotic fluid and parental blood samples.
6,440 THB
Add to WishlistRemove from Wishlist
Add to Wishlist
