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Results: 21 to 40 of 49

Tests names and labsConditionsGenes, analytes, and microbesMethods

SH3TC2

Institute for Human Genetics University Medical Center Freiburg
Germany
21
  • C Sequence analysis of the entire coding region

SH3TC2 - Gene sequencing

Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center, Location AMC
Netherlands
21
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth Panel, Comprehensive

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
8530
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth disease: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
6754
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth Hereditary Neuropathy NGS Panel

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

Paroxysmal Extreme Pain Disorder NGS Panel

Fulgent Genetics
United States
18553
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth Disease Type 4 , Panel Massive Sequencing (NGS) 11 Genes

Reference Laboratory Genetics
Spain
1111
  • 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

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 DISEASE TYPE 4C

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

Charcot-Marie-Tooth Disease Type 4 , Deletions-Duplications (MLPA) GDAP1,MTMR2,SBF2,PRX,SH3TC2 Genes

Reference Laboratory Genetics
Spain
55
  • D Deletion/duplication analysis

Charcot-Marie-Tooth Disease Type 4C, Sequencing SH3TC2 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

CMT Advanced Evaluation - Nonprevalent Demyelinating

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

CMT Advanced Evaluation - Nonprevalent

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

Charcot-Marie-Tooth disease type 4C

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

Charcot-Marie-Tooth and Sensory Neuropathies Panel

CeGaT GmbH
Germany
6384
  • C Sequence analysis of the entire coding region

SH3TC2

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

Charcot-Marie-Tooth Disease

Asper Biogene Asper Biogene LLC
Estonia
8974
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SH3TC2 Single Gene

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 49

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.