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Results: 1 to 4 of 4

Tests names and labsConditionsGenes, analytes, and microbesMethods

Corneal dystrophy, Fuchs endothelial, 8, 615523, Autosomal dominant; FECD8 (Fuchs endothelial corneal dystrophy) (AGBL1 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

Anterior Segment Dysgenesis Disorders Panel

PreventionGenetics, part of Exact Sciences
United States
272278
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Corneal Dystrophies Panel

PreventionGenetics, part of Exact Sciences
United States
4027
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Corneal dystrophy: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
1911
  • C Sequence analysis of the entire coding region

Results: 1 to 4 of 4

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