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Results: 61 to 80 of 84

Tests names and labsConditionsGenes, analytes, and microbesMethods

Beacon Expanded Female Carrier Screening Plus Panel

Fulgent Genetics
United States
716335
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon ACOG/ACMG Female Carrier Screening Panel

Fulgent Genetics
United States
166
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Female Carrier Screening Panel

Fulgent Genetics
United States
690326
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Focus Female Carrier Screening Panel

Fulgent Genetics
United States
5330
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Fragile X-associated tremor/ataxia syndrome

Molecular Genetics Laboratory North York General Hospital
Canada
11
  • T Targeted variant analysis

Fragile X tremor/ataxia syndrome

Labor Dr. Wisplinghoff
Germany
11
  • T Targeted variant analysis

Fragile X mutation analysis by PCR

Diagnostics Division CENTRE FOR DNA FINGERPRINTING AND DIAGNOSTICS
India
11
  • X Mutation scanning of select exons

Hereditary Ataxia

Asper Biogene Asper Biogene LLC
Estonia
180139
  • C Sequence analysis of the entire coding region

Fragile X syndrome

Bioarray
Spain
11
  • D Deletion/duplication analysis

Fragile X Syndrome, FMR1

MVZ Dr. Eberhard & Partner Dortmund
Germany
31
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

FMR1 Single Gene

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Fragile X (FMR1) with Reflex to Methylation Analysis, Fetal

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
21
  • M Methylation analysis
  • T Targeted variant analysis

Fragile X (FMR1) with Reflex to Methylation Analysis

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
21
  • M Methylation analysis
  • T Targeted variant analysis

Clinical Exome

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

XLID (X-Linked Intellectual Disability) NGS Panel

Fulgent Genetics
United States
162117
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1058554
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Autism NGS Panel

Fulgent Genetics
United States
170106
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FMR1-Related Disorders

Molecular Genetics Laboratory BC Children's and BC Women's Hospitals
Canada
31
  • T Targeted variant analysis

FMR1-Related Disorders

MGZ Medical Genetics Center
Germany
31
  • D Deletion/duplication analysis
  • M Methylation analysis
  • T Targeted variant analysis

Fragile X-Associated Tremor Ataxia Syndrome (FXTAS)

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
11
  • T Targeted variant analysis

Results: 61 to 80 of 84

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.