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Test Code 11735

Craniosynostosis via the TCF12 Gene

TCF12

N/A

Who is this test for?

Candidates for this test are patients with symptoms consistent with Craniosynostosis, and the family members of patients who have known TCF12 pathogenic variants (Bravenboer et al. 2015).

Method
Sequencing with CNV PGxome
Specimen(s)

Blood, Saliva, or Buccal Swab

Order Options

Platform
Test type
OTHER OPTIONS
for standard institutional pricing.

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