Test Code 959
Craniosynostosis via the MSX2 Gene
MSX2
N/A
Who is this test for? | Candidates for this test are patients with symptoms consistent with Craniosynostosis, Parietal foramina 1, Parietal foramina with cleidocranial dysplasia and the family members of patients who have known MSX2 pathogenic variants. |
Method | Sanger Sequencing |
Specimen(s) | Blood, Saliva, or Buccal Swab |
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