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Test Code 10491

Hypogonadotropic Hypogonadism/Kallmann Syndrome via the CCDC141 Gene

CCDC141

N/A

Who is this test for?

Candidates for this test are patients with symptoms consistent with hypogonadotropic hypogonadism/Kallmann syndrome.

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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