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Results: 1 to 8 of 8

Tests names and labsConditionsGenes, analytes, and microbesMethods

Adult i phenotype without cataract, 110800, Autosomal dominant (GCNT2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

MVL Vision Panel

Molecular Vision Laboratory
United States
13581028
  • C Sequence analysis of the entire coding region

GCNT2 - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CentoVision Panel

Centogene AG - the Rare Disease Company
Germany
417413
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cataracts Panel

PreventionGenetics, part of Exact Sciences
United States
161174
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Cataract panel. NGS panel of 69 genes.

Genologica Medica
Spain
14669
  • C Sequence analysis of the entire coding region

Single gene testing GCNT2

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Cataract Panel

CeGaT GmbH
Germany
2441
  • C Sequence analysis of the entire coding region

Results: 1 to 8 of 8

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