Filters

See more specimen types...
See more states

Other countries

See more countries

Results: 1 to 20 of 721

Tests names and labsConditionsGenes, analytes, and microbesMethods

NGS panel - Ehlers-Danlos syndromes (Ehlers-Danlos type IV - vascular type - excluded)

Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center
Netherlands
1522
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region
  • T Targeted variant analysis

Ehlers-Danlos Syndromes Panel

PreventionGenetics
United States
9864
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ehlers-Danlos, Marfan and Loeys-Dietz syndromes, aortic aneurysm and differential diagnosis (WES based NGS panel of 77 genes, including CNV analysis)

CGC Genetics
Portugal
15977
  • C Sequence analysis of the entire coding region

Invitae Ehlers-Danlos Syndrome Panel

Invitae
United States
3817
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ehlers-Danlos Syndrome

Asper Biogene Asper Biogene LLC
Estonia
6937
  • C Sequence analysis of the entire coding region

Ehlers-Danlos syndrome: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
2020
  • C Sequence analysis of the entire coding region

Ehlers-Danlos Syndrome Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
1312
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Connective Tissue Disorders Panel

PreventionGenetics
United States
15493
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ehlers Danlos Syndrome Panel

CNMC Molecular Diagnostics Laboratory Childrens National Medical Center
United States
3114
  • C Sequence analysis of the entire coding region

Ehlers-Danlos Syndrome NGS Panel

Fulgent Genetics
United States
9721
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

EHLERS-DANLOS SYNDROME: NGS PANEL-2

Laboratorio de Genetica Clinica SL
Spain
1315
  • C Sequence analysis of the entire coding region

NGS panel - Ehlers-Danlos syndromes (Ehlers-Danlos type IV - vascular type - excluded) + FN1

Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center
Netherlands
1323
  • D Deletion/duplication analysis
  • T Targeted variant analysis

EHLERS-DANLOS, SYNDROME

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1111
  • C Sequence analysis of the entire coding region

Ehlers-Danlos syndrome Comprehensive panel - Dominant & Recessive

Connective Tissue Gene Tests
United States
1420
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ehlers-Danlos syndrome Deletion / Duplication panel - Dominant & Recessive

Connective Tissue Gene Tests
United States
1420
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ehlers-Danlos syndrome NGS panel - Dominant & Recessive

Connective Tissue Gene Tests
United States
1420
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ehlers-Danlos syndrome Comprehensive panel - Dominant & Recessive

Connective Tissue Gene Tests
United States
1420
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ehlers-Danlos syndrome Deletion / Duplication panel - Dominant & Recessive

Connective Tissue Gene Tests
United States
1420
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ehlers-Danlos syndrome NGS panel - Dominant & Recessive

Connective Tissue Gene Tests
United States
1420
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Connective tissue disorders - Ehlers-Danlos syndrome, Marfan syndrome, Loeys-Dietz syndrome, Aortic Aneurysm

CeGaT GmbH
Germany
3844
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 721

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.

Support Center