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Results: 1 to 20 of 20

Tests names and labsConditionsGenes and analytesMethods

AllNeuro panel

Centogene AG - the Rare Disease Company
Germany
7861205
  • C Sequence analysis of the entire coding region

Myotonic dystrophy type 2

Centogene AG - the Rare Disease Company
Germany
11
  • E Sequence analysis of select exons

CNBP. CCTG expansion detection by PCR

Instituto de Medicina Genomica
Spain
11
  • T Targeted variant analysis

ZNF9. CCTG expansion detection by PCR

Instituto de Medicina Genomica
Spain
11
  • T Targeted variant analysis

MYOTONIC DYSTROPHY TYPE 2

Laboratorio de Genetica Clinica SL
Spain
11
  • T Targeted variant analysis

Neuromuscular Comprehensive Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
454305
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Myotonic Syndrome Advanced Evaluation

Athena Diagnostics Inc
United States
97
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Proximal myotonic myopathy

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Myotone Dystrophy Type 2

MVZ Dortmund Dr. Eberhard and Partner
Germany
11
  • E Sequence analysis of select exons

Myotone Dystrophy Type 2

MVZ Dortmund Dr. Eberhard and Partner
Germany
11
  • E Sequence analysis of select exons

CNBP

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CNBP DNA Test (DM2)

Athena Diagnostics Inc
United States
11
  • T Targeted variant analysis

Myotonic dystrophy II

Praxis fuer Humangenetik Wien
Austria
11
  • T Targeted variant analysis

Myotonic dystrophy type 2: ZNF9 gene expansion analysis

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • C Sequence analysis of the entire coding region

Myotonic Dystrophy Type 2

Medizinisch Genetisches Zentrum München MGZ München
Germany
11
  • T Targeted variant analysis

Test for Myotonic Dystrophy Type 2

All Wales Genetics Laboratory Institute of Medical Genetics
United Kingdom
11
  • T Targeted variant analysis

Myotonic Dystrophy type 2

Neuromuscular Research Unit, Neurogenetics University of Tampere
Finland
11
  • T Targeted variant analysis

Myotonic dystrophy type 2 (CCTG expansion on ZNF9 gene)

CGC Genetics
Portugal
11
  • T Targeted variant analysis

Myotonic Dystrophy Type 2

Clinical Genomics Maastricht University Medical Centre
Netherlands
11
  • T Targeted variant analysis

Myotonic dystrophy type II

Synlab MVZ Humane Genetik München
Germany
11
  • T Targeted variant analysis

Results: 1 to 20 of 20

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.

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