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Results: 1 to 20 of 45

Tests names and labsConditionsGenes and analytesMethods

CMT2E

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region

Charcot-Marie-Tooth Type 2E/1F via the NEFL Gene

PreventionGenetics
United States
21
  • 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 - Axonal Neuropathy Sequencing Panel

PreventionGenetics
United States
4738
  • 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 Panel

Molecular Genetics Laboratory London Health Sciences Centre
Canada
4634
  • 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

DNM2, GARS, GDAP1, GJB1, MFN2, MPZ, MTMR2, NEFL, PMP22, PRX. NextGeneDx.Complete sequencing by NGS

Instituto de Medicina Genomica
Spain
1810
  • C Sequence analysis of the entire coding region

NEFL. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • 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

Charcot-Marie-Tooth Disease Type 2 , Panel Massive Sequencing (NGS) 20 Genes

Reference Laboratory Genetics
Spain
2420
  • C Sequence analysis of the entire coding region

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

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 DISEASE TYPE 2E

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

NEFL

Institute for Human Genetics University Clinic Freiburg
Germany
21
  • 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

Results: 1 to 20 of 45

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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