Genetic Disease Test

  • To understand the risk of family genetic diseases
  • To analyze the specific disease
  • To test whether you have any genetic disease
  • To predict specific disease
  • To understand your own health
  • Fragile X syndrome (FMR1)
  • Spinal Muscular Atrophy (PCR+MLPA)
  • Thalassemia (α+β)
  • Huntington’s disease (PCR)
  • Congenital central hypoventilation syndrome (PHOX2B)
  • Marfan syndrome (FBN1,TGFBR1, TGBR2)
  • Duchenne Muscular Dystrophy (DNA Sequence default)
  • Duchenne Muscular Dystrophy (single point mutation)
  • Cystic Fibrosis (10 hot spots)
  • Cystic Fibrosis (CFTR whole gene)