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Results: 1 to 20 of 29 (representing 14 labs)

Tests names and labsConditionsGenes and analytesMethods

Fanconi anemia type F

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Fanconi Anemia Sequencing Panel

Genetic Services Laboratory University of Chicago
United States
1918
  • C Sequence analysis of the entire coding region

Fanconi Anemia via the FANCF Gene

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Fanconi Anemia Sequencing Panel

PreventionGenetics
United States
1719
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Chromosomes, DEB Assay for Fanconi Anemia

Quest Diagnostics Nichols Institute Chantilly
United States
1515
  • B Chromosome breakage studies

Chromosome DEB Assay for Fanconi anemia, Prenatal

Quest Diagnostics Nichols Institute Chantilly
United States
1515
  • B Chromosome breakage studies

Fanconi Anemia

Asper Biotech Asper Biotech Ltd.
Estonia
1717
  • C Sequence analysis of the entire coding region

Invitae Bone Marrow Failure Syndromes Panel

Invitae
United States
4939
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ONCOLOGY, PANEL

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
6780
  • C Sequence analysis of the entire coding region

Fanconi anemia

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1416
  • C Sequence analysis of the entire coding region

FANCF - Gene sequencing

Genome Diagnostics VU University Medical Center
Netherlands
11
  • E Sequence analysis of select exons
  • T Targeted variant analysis

Fanconi anemia - Sequencing panel

Genome Diagnostics VU University Medical Center
Netherlands
56
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • T Targeted variant analysis

Fanconi anemia Panel

CeGaT GmbH
Germany
1716
  • C Sequence analysis of the entire coding region

Fanconi anemia type F (sequence analysis of FANCF gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

FANCF Deletion/duplication analysis

Molecular Genetics Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • D Deletion/duplication analysis

Cancer Predisposition

Asper Biotech Asper Biotech Ltd.
Estonia
12789
  • C Sequence analysis of the entire coding region

Fanconi Anemia Deletion/Duplication Panel

Molecular Genetics Laboratory Cincinnati Children's Hospital Medical Center
United States
1615
  • D Deletion/duplication analysis

Bone Marrow Failure Syndromes Deletion/Duplication Panel

Molecular Genetics Laboratory Cincinnati Children's Hospital Medical Center
United States
4355
  • D Deletion/duplication analysis

FANCF

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

Invitae Fanconi Anemia Panel

Invitae
United States
1717
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 29

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.

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