How does genetic testing work?


 

  • Direct Testing: Screens DNA sequences for unknown mutations, or tests specific DNA for a known mutation

     

  • Linkage Testing: Looks at markers co-inherited with a disease-causing gene

     

  • Biochemical Testing: Screens urine, plasma, red/white blood cells, or placental tissue or amniocyte samples to evaluate metabolic diseases and enzymatic function.

     

  • Cytogenetic Testing: Uses white blood cells, amniocytes, chorionic villus samples, miscarried fetuses, and skin biopsies to examine chromosomes

     

  


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