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Results: 1 to 7 of 7

Tests names and labsConditionsGenes, analytes, and microbesMethods

PDCD1 - NGS including CNV analysis

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

CentoNeuro Panel

Centogene AG - the Rare Disease Company
Germany
18861858
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability Panel

Centogene AG - the Rare Disease Company
Germany
777770
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Multiple sclerosis, susceptibility to, 1, 126200, Multifactorial (Sporadic Creutzfeldt-Jakob disease) (HLA-DQB1 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

Multiple sclerosis, susceptibility to, 1, 126200, Multifactorial (HLA-DRB1 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

Multiple sclerosis, disease progression, modifier of, 126200, Multifactorial (PDCD1 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

TNFRSF1A Select Exons Sequencing

GeneDx
United States
31
  • E Sequence analysis of select exons

Results: 1 to 7 of 7

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