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Results: 41 to 55 of 55

Tests names and labsConditionsGenes, analytes, and microbesMethods

Ataxia and differential diagnoses Panel

CeGaT GmbH
Germany
173204
  • C Sequence analysis of the entire coding region

Choreatic Movement Disorders Panel

CeGaT GmbH
Germany
1621
  • C Sequence analysis of the entire coding region

Parkinson all Panel

CeGaT GmbH
Germany
4248
  • C Sequence analysis of the entire coding region

SCA3

Molecular Diagnostics Laboratory Seoul National University Hospital
South Korea
11
  • X Mutation scanning of select exons

Spinocerebellar ataxia 3

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • X Mutation scanning of select exons

ATXN3 Single Gene

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

SCA3 (MJD/ATXN3) Repeat Expansion Test

Athena Diagnostics Inc
United States
11
  • T Targeted variant analysis

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • 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

Spinocerebellar Ataxia Panel (SCA1, SCA2, SCA3, SCA6, SCA7)

Molecular Genetics Laboratory BC Children's and BC Women's Hospitals
Canada
55
  • T Targeted variant analysis

Spinocerebellar ataxia 3

Center for Human Genetics, Inc
United States
11
  • T Targeted variant analysis

Spinocerebellar Ataxia 03

Praxis fuer Humangenetik Wien
Austria
11
  • T Targeted variant analysis

Spinocerebellar Ataxia Type 3

MGZ Medical Genetics Center
Germany
11
  • T Targeted variant analysis

SCA 3

Institute of Medical Genetics and Genomics Sir Ganga Ram Hospital
India
11
  • T Targeted variant analysis

Spinocerebellar Ataxia: Panel of SCA1, SCA2, SCA3, SCA6, SCA7

Defense Health Agency Genetics Reference Laboratory United States Air Force
United States
55
  • T Targeted variant analysis

Results: 41 to 55 of 55

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.