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Results: 21 to 39 of 39

Tests names and labsConditionsGenes, analytes, and microbesMethods

Frontotemporal Dementia, Chromosome 3-Linked: gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

Frontotemporal Dementia , Panel Massive Sequencing (NGS) 8 Genes

Reference Laboratory Genetics
Spain
88
  • C Sequence analysis of the entire coding region

AMYOTROPHIC LATERAL SCLEROSIS (ALS) (AUTOSOMAL DOMINANT)

Laboratorio de Genetica Clinica SL
Spain
1417
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Amyotrophic Lateral Sclerosis

Asper Biogene Asper Biogene LLC
Estonia
2222
  • C Sequence analysis of the entire coding region

Frontotemporal Dementia , Sequencing CHMP2B Gene

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

Nonprevalent Amyotrophic Lateral Sclerosis Advanced Sequencing Evaluation

Athena Diagnostics Inc
United States
2415
  • C Sequence analysis of the entire coding region

Amyotrophic Lateral Sclerosis Advanced Evaluation

Athena Diagnostics Inc
United States
1917
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Frontotemporal Dementia

Asper Biogene Asper Biogene LLC
Estonia
2920
  • C Sequence analysis of the entire coding region

NGS panel - dementia/ALS

Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center
Netherlands
4254
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region
  • T Targeted variant analysis

FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED

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

Single gene testing CHMP2B

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Dementia all Panel

CeGaT GmbH
Germany
3236
  • C Sequence analysis of the entire coding region

Frontotemporal Dementia (FTD) Panel

CeGaT GmbH
Germany
2928
  • C Sequence analysis of the entire coding region

Amyotrophic Lateral Sclerosis (ALS) Panel

CeGaT GmbH
Germany
2954
  • 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

CHMP2B Single Gene

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

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FTD - ALS panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
2815
  • C Sequence analysis of the entire coding region

Amyotrophic Lateral Sclerosis NGS Panel

Fulgent Genetics
United States
8443
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 39 of 39

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.