U.S. flag

An official website of the United States government

Filters

See more specimen types...

Other countries

Results: 1 to 11 of 11

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hemophilia B, F9 Gene, Full Gene Next-Generation Sequencing

Mayo Clinic Laboratories Mayo Clinic
United States
31
  • C Sequence analysis of the entire coding region

Hemophilia A, F8 Gene, Full Gene Next-Generation Sequencing

Mayo Clinic Laboratories Mayo Clinic
United States
21
  • C Sequence analysis of the entire coding region

Hemophilia A, sequencing

Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS
Chile
11
  • E Sequence analysis of select exons

Hemophilia A (F8) Sequencing

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
51
  • C Sequence analysis of the entire coding region

Mutation analysis of Intron 22 inversion mutation in F8 gene for Hemoplilia A

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

Comprehensive Bleeding Disorder Panel

Versiti Diagnostic Laboratories Versiti, Inc
United States
8050
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Factor IX (Hemophilia B) Genetic Analysis

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
21
  • C Sequence analysis of the entire coding region

Factor VIII (Hemophilia A) Genetic Analysis

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
21
  • C Sequence analysis of the entire coding region

X Inactivation

Genetic Diagnostic Laboratory University of Pennsylvania School of Medicine
United States
31
  • M Methylation analysis

Bleeding Disorder/Coagulopathy Panel

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

Hemophilia A

Genetic Diagnostic Laboratory University of Pennsylvania School of Medicine
United States
21
  • D Deletion/duplication analysis
  • L Linkage analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Results: 1 to 11 of 11

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.