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Results: 1 to 8 of 8

Tests names and labsConditionsGenes, analytes, and microbesMethods

CX3CR1 - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Macular degeneration, age-related, 12, 613784; ARMD12 (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Macular degeneration, age-related, 12, 613784; ARMD12 (CX3CR1 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

Macular degeneration, age-related: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
1517
  • C Sequence analysis of the entire coding region

Macular Degeneration Related Disorders , Panel Massive Sequencing (NGS) 15 Genes

Reference Laboratory Genetics
Spain
1515
  • C Sequence analysis of the entire coding region

CX3CR1 Single Gene

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Macular Degeneration NGS Panel

Fulgent Genetics
United States
5319
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 8 of 8

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