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Results: 41 to 60 of 60

Tests names and labsConditionsGenes, analytes, and microbesMethods

Ataxia, Supplemental Recessive Evaluation

Athena Diagnostics Inc
United States
2017
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Oculomotor Apraxia Ataxia Advanced Sequencing Evaluation

Athena Diagnostics Inc
United States
32
  • C Sequence analysis of the entire coding region

Ataxia, autosomal recessive and X-linked Panel

CeGaT GmbH
Germany
746
  • C Sequence analysis of the entire coding region

Spinocerebellar ataxia with axonal neuropathy type 2

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

Single gene testing SETX

CeGaT GmbH
Germany
21
  • C Sequence analysis of the entire coding region

Leukodystrophy / Leukencephalopathy and differential diagnoses Panel

CeGaT GmbH
Germany
69175
  • C Sequence analysis of the entire coding region

Ataxia and differential diagnoses Panel

CeGaT GmbH
Germany
173204
  • 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

SETX Single Gene

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

Distal Hereditary Motor Neuropathy NGS Panel

Fulgent Genetics
United States
3815
  • 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

Ataxia (AD/AR) panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
2316
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Amyotrophic Lateral Sclerosis NGS Panel

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

Spinocerebellar Ataxia, autosomal recessive 1

MedGene
Slovakia
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ataxia with Oculomotor Apraxia 2

MedGene
Slovakia
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Spinocerebellar Ataxia, autosomal recessive 1

Praxis fuer Humangenetik Wien
Austria
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ataxia with Oculomotor Apraxia 2

Praxis fuer Humangenetik Wien
Austria
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ataxia with Oculomotor Apraxia 2

MGZ Medical Genetics Center
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 41 to 60 of 60

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.