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Results: 81 to 92 of 92

Tests names and labsConditionsGenes, analytes, and microbesMethods

Coagulation Factor Deficiency Panel

Blueprint Genetics
Finland
316
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bleeding Disorder/Coagulopathy Panel

Blueprint Genetics
Finland
762
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hemophilia B

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

Hemophilia B (F9) Targeted Testing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
11
  • T Targeted variant analysis

F9 Single Gene

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

Coagulation Deficiency NGS Panel

Fulgent Genetics
United States
5624
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

F9 Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
31
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hemophilia B

Center for Human Genetics Cliniques Universitaires Saint Luc
Belgium
11
  • C Sequence analysis of the entire coding region

Hemophilia B

Genetic Diagnostic Laboratory University of Pennsylvania School of Medicine
United States
21
  • L Linkage analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Hemophilia B

Diagenom GmbH
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hemophila B

Institute of Medical Genetics and Genomics Sir Ganga Ram Hospital
India
11
  • L Linkage analysis
  • S Mutation scanning of the entire coding region

Results: 81 to 92 of 92

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.