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Results: 21 to 40 of 85

Tests names and labsConditionsGenes, analytes, and microbesMethods

Ataxia Exome

Genetic Services Laboratory University of Chicago
United States
289481
  • C Sequence analysis of the entire coding region

Fragile X Syndrome, Diagnostic

Molecular Diagnostic Laboratory LabCorp
United States
31
  • T Targeted variant analysis

X-Linked Intellectual Disability Panel

PreventionGenetics, part of Exact Sciences
United States
191141
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

FMR1 Sequence Analysis (Prenatal Diagnosis)

Baylor Genetics
United States
31
  • T Targeted variant analysis

FMR1 Sequence Analysis (Familial Mutation/Variant Analysis)

Baylor Genetics
United States
31
  • T Targeted variant analysis

FMR1 Sequence Analysis

Baylor Genetics
United States
31
  • C Sequence analysis of the entire coding region

Fragile X Syndrome via the FMR1 CGG Repeat Expansion

PreventionGenetics, part of Exact Sciences
United States
31
  • M Methylation analysis
  • I Microsatellite instability testing (MSI)

XSense(R), Fragile X with Reflex

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
21
  • M Methylation analysis

Fragile X Tremor/Ataxia Syndrome

UCSF Molecular Diagnostics Laboratory University of California, San Francisco
United States
10
  • M Methylation analysis
  • T Targeted variant analysis

FMR1-Related Disorders

University of Iowa Diagnostic Laboratories University of Iowa Hospitals and Clinics
United States
31
  • M Methylation analysis
  • T Targeted variant analysis

Fragile X Mutation

Molecular Diagnostic Laboratory Nebraska Medicine
United States
31
  • T Targeted variant analysis

Fragile X syndrome

Molecular Diagnostic Laboratory Diagnostic Services, Shared Health Manitoba
Canada
31
  • T Targeted variant analysis

Fragile X syndrome (FXS), Primary ovarian insufficiency (FXPOI), Fragile X-associated tremor/ataxia syndrome (FXTAS) (FMR1 gene analysis by msTP-PCR) 

CGC Genetics Unilabs
Portugal
31
  • M Methylation analysis

Fragile X syndrome (FXS), Primary ovarian insufficiency (FXPOI), Fragile X-associated tremor/ataxia syndrome (FXTAS) (FMR1 gene analysis by conventional PCR) 

CGC Genetics Unilabs
Portugal
31
  • T Targeted variant analysis

Beacon Carrier Screen; 3 Genes

Fulgent Genetics
United States
53
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Periventricular heterotopia panel

Genologica Medica
Spain
5220
  • C Sequence analysis of the entire coding region

Hereditary ataxias. NGS panel of 139 genes.

Genologica Medica
Spain
220139
  • C Sequence analysis of the entire coding region

Ataxia panel. NGS panel of 157 genes.

Genologica Medica
Spain
247156
  • C Sequence analysis of the entire coding region

X-linked intellectual disability panel. 99-gene NGS panel.

Genologica Medica
Spain
14399
  • C Sequence analysis of the entire coding region

Fragile X Repeat Analysis

Duzen Laboratories Duzen BBAGUAS
Turkey
31
  • T Targeted variant analysis

Results: 21 to 40 of 85

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.