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Peutz-Jeghers Syndrome
STK11 (Serine/threonine protein kinase II)
Mutations in STK11 are identified by complete sequence analysis of the coding region of the gene. The analysis is done on genomic DNA from buccal swabs. Pre-symptomatic diagnosis is available.
Information Sheet, including prices and CPT codes
Consent Document
Genetic Test Sample Submission Form (Test Requisition Form) including Payment Options
PJ, PJS, STK11, polyposis, hamartomatous intestinal polyposis, LKB
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