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Test Code 5000

PGxome® - Whole Exome Test

3 - 5 weeks

Who is this test for?
  • Individuals with congenital anomalies, intellectual disability, developmental delay, autism spectrum disorder, and/or unexplained epilepsy 
  • Individuals who have a suspected diagnosis associated with significant genetic heterogeneity 
  • Individuals with clinical features suggestive of an underlying genetic diagnosis that do not align with a well-defined syndrome 
  • Individuals with previously unresolved genetic testing 
  • Non-ongoing fetal cases with a suspected underlying genetic cause 
Method
Exome Platform with CNV
Specimen(s)

Blood, Buccal, Saliva, Tissue

Order Options

Test type
OTHER OPTIONS
for pricing.

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