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Results: 1 to 20 of 35

Tests names and labsConditionsGenes and analytesMethods

AllNeuro panel

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

DI-CMTC

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth Autosomal Dominant Intermediate C via the YARS Gene

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Comprehensive Neuropathy Sequencing Panel

PreventionGenetics
United States
8271
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Charcot Marie Tooth - Comprehensive Sequencing Panel

PreventionGenetics
United States
5445
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Charcot Marie Tooth - Demyelinating Neuropathy Sequencing Panel

PreventionGenetics
United States
3525
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Charcot-Marie-Tooth

Human Genetics University Hospital Bern
Switzerland
2322
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Neuropathies: Deletion/Duplication Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
12790
  • D Deletion/duplication analysis

Motor Neuron Disorder and Related Diseases , Panel Massive Sequencing (NGS) 49 Genes

Reference Laboratory Genetics
Spain
6049
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth Disease, Panel Massive Sequencing (NGS) 32 Genes

Reference Laboratory Genetics
Spain
4132
  • C Sequence analysis of the entire coding region

Hereditary Peripheral Neuropathy , Panel Massive Sequencing (NGS) 31 Genes

Reference Laboratory Genetics
Spain
4131
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth Hereditary Neuropathy Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
7654
  • C Sequence analysis of the entire coding region

CHARCOT-MARIE-TOOTH : NGS PANEL

Laboratorio de Genetica Clinica SL
Spain
4034
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth neuropathy axonal autosomal dominant panel

LifeLabs Genetics
Canada
2318
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CMT Advanced Evaluation - Nonprevalent Axonal

Athena Diagnostics Inc
United States
1311
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CMT Advanced Evaluation - Nonprevalent Demyelinating

Athena Diagnostics Inc
United States
1714
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CMT Advanced Evaluation - Nonprevalent

Athena Diagnostics Inc
United States
2521
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Comprehensive Neuropathies Panel

Invitae
United States
10070
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CHARCOT- MARIE TOOTH

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
3432
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth and Sensory Neuropathies Panel

CeGaT GmbH
Germany
6484
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 35

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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