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Test Code 8491

Premature Ovarian Failure/Ovarian Dysgenesis via the SOHLH1 Gene

SOHLH1

N/A

Who is this test for?

This test is for patients with premature ovarian failure/Ovarian dysgenesis. Testing is also indicated for family members of patients who have known SOHLH1 pathogenic variants. This test may also be considered for the reproductive partners of individuals who carry pathogenic variants in SOHLH1.

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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