Lissencephaly 2 (Norman-Roberts type), 257320, Autosomal recessive; LIS2 (Lissencephaly syndrome, Norman-Roberts type) (RELN gene) (Sequence Analysis-All Coding Exons) (Postnatal)
- GTR Test IDHelpEach Test is a specific, orderable test from a particular laboratory, and is assigned a unique GTR accession number. The format is GTR00000001.1, with a leading prefix 'GTR' followed by 8 digits, a period, then 1 or more digits representing the version. When a laboratory updates a registered test, a new version number is assigned.: GTR000582162.1
- Last updated: 2020-05-19
- Annual Review past due read more
- Test version history
- 582162.1, last updated: 2020-05-19
Clinical testHelpIn the U.S., clinical tests must be performed under CLIA certification. When a lab uses the same methods for a test in both clinical and research settings, the test appears as two separate GTR records. for Norman-Roberts syndrome
Offered by Intergen
Overview
Test name
HelpThe name the laboratory assigns the test. Used as the default title of the page specific to the test.Lissencephaly 2 (Norman-Roberts type), 257320, Autosomal recessive; LIS2 (Lissencephaly syndrome, Norman-Roberts type) (RELN gene) (Sequence Analysis-All Coding Exons) (Postnatal)
This is a clinical test intended for HelpPurposes or indications for the test. Lab-provided.: Diagnosis
Click Indication tab for more information.
Not provided
Methodology
HelpThe assay's major method category (biochemical, cytogenetic or molecular genetics); method category (i.e. enzyme assay, chromosome breakage studies, targeted mutation analysis); methodology (i.e. the name of the method used) and instruments used when performing this test.- Molecular Genetics
- CSequence analysis of the entire coding region
- Next-Generation (NGS)/Massively parallel sequencing (MPS)
Not provided
Clinical validity
HelpHow consistently and accurately the test detects or predicts the intermediate or final outcomes of interest. Lab-provided.Not provided
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