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Results: 1 to 20 of 34

Tests names and labsConditionsGenes and analytesMethods

AllNeuro panel

Centogene AG - the Rare Disease Company
Germany
6021038
  • C Sequence analysis of the entire coding region

CMT2F

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

Charcot Marie Tooth - Axonal Neuropathy NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
5041
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Charcot Marie Tooth - Comprehensive NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
5445
  • 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
3017
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

TruGenome Predisposition Screen (Whole Genome Sequencing)

Illumina Clinical Services Laboratory Illumina
United States
15411578
  • C Sequence analysis of the entire coding region

HSPB1. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

Distal Hereditary Motor Neuropathy NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
2217
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Heat Shock 27 kDa Protein-Related Disorders via the HSPB1 Gene

PreventionGenetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

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 neuropathy type 2F

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

Charcot-Marie-Tooth disease (NGS panel for 43 genes)

CGC Genetics
Portugal
2443
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth disease type 2F (CMT2F, sequence analysis of HSPB1 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

Spinal Muscular Atrophy (SMA) Panel

CeGaT GmbH
Germany
4427
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth and Sensory Neuropathies Panel

CeGaT GmbH
Germany
6584
  • C Sequence analysis of the entire coding region

Hereditary Spastic Paraplegias (HSP) and differential diagnoses Panel

CeGaT GmbH
Germany
147143
  • C Sequence analysis of the entire coding region

HSPB1 - Gene sequencing

Clinical Genetics Academic Medical Center
Netherlands
21
  • C Sequence analysis of the entire coding region

HSPB1

Division Human Genetics Medical University Innsbruck
Austria
21
  • S Mutation scanning of the entire coding region

Charcot-Marie-Tooth Disease

Asper Biotech Asper Biotech Ltd.
Estonia
4530
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth: Sequencing HSPB1 gene

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

Results: 1 to 20 of 34

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.