Filters

See more specimen types...

Other countries

Results: 1 to 20 of 23 (representing 12 labs)

Tests names and labsConditionsGenes and analytesMethods

Dementia Sequencing Panel

PreventionGenetics
United States
1213
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Amyotrophic Lateral Sclerosis and Frontotemporal Dementia via the CHMP2B Gene

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

TARDBP. Complete sequencing

Instituto de Medicina Genomica
Spain
31
  • C Sequence analysis of the entire coding region

MAPT, GRN. MLPA testing

Instituto de Medicina Genomica
Spain
32
  • D Deletion/duplication analysis

Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Sequencing Panel

PreventionGenetics
United States
1721
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

MAPT. Sequencing of the exons 1, 9, 10, 11, 12 and 13

Instituto de Medicina Genomica
Spain
31
  • E Sequence analysis of select exons

GRN. Complete sequencing

Instituto de Medicina Genomica
Spain
31
  • C Sequence analysis of the entire coding region

MAPT. Complete sequencing

Instituto de Medicina Genomica
Spain
31
  • 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

Frontotemporal dementia

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
88
  • C Sequence analysis of the entire coding region

Frontotemporal dementia: CHMP2B gene sequence analysis

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

Frontotemporal Dementia

Asper Biotech Asper Biotech Ltd.
Estonia
44
  • C Sequence analysis of the entire coding region

NGS panel - dementia

Genome Diagnostics VU University Medical Center
Netherlands
2341
  • 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
21
  • 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

Frontotemporal Lobar Degeneration (CHMP2B gene)

Diagnostic Service Facility University of Antwerp
Belgium
11
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 23

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.

Support Center