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Test Code 9059

Amelogenesis Imperfecta via the ODAPH (C4orf26) Gene

ODAPH

N/A

Who is this test for?

Candidates for this test are patients with symptoms consistent with autosomal recessive hypomineralized amelogenesis imperfecta and the family members of patients who have known ODAPH mutations. This test may also be considered for the reproductive partners of individuals who carry pathogenic variants in ODAPH.

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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