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Results: 1 to 20 of 55

Tests names and labsConditionsGenes and analytesMethods

CentoICU platinum

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

Rapid microarray (CGH and SNP)

Allele Diagnostics
United States
247231
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Hemophilia A

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

DNA Hemophilia A mutation evaluation

Genomics - Bleeding Disorders BloodworksNW
United States
11
  • L Linkage analysis
  • S Mutation scanning of the entire coding region
  • E Sequence analysis of select exons

Hemophilia A

Molecular Genetics and Cytogenetics, Clinical Laboratory Service Faculty of Medicine, Pontificia Universidad Católica de Chile
Chile
11
  • D Deletion/duplication analysis

Factor VIII mutation analysis

DNA Diagnostics Laboratory Academic Medical Centre, University of Amsterdam
Netherlands
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Haemophilia A

GENETIX Centro de Investigación en Genética Humana y Reproductiva
Colombia
11
  • L Linkage analysis

Hemophilia A via the F8 gene

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

F8. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

F8. Detection of the intron 22 inversion

Instituto de Medicina Genomica
Spain
11
  • T Targeted variant analysis

Bleeding Disorders Sequencing Panel

PreventionGenetics
United States
5561
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Coagulation Factor Deficiency Sequencing Panel

PreventionGenetics
United States
2120
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

FVIII Inversions

Genomics - Bleeding Disorders BloodworksNW
United States
11
  • S Mutation scanning of the entire coding region

Hemophilia A: Prenatal Diagnosis

Foundation for Research In Genetics and Endocrinology and Institute of Human Genetics Institute of Human Genetics
India
11
  • T Targeted variant analysis

Hemophilia A:Carrier analysis for intragenic markers (Bcl1, Xbal, In 13 and 22)

Foundation for Research In Genetics and Endocrinology and Institute of Human Genetics Institute of Human Genetics
India
11
  • T Targeted variant analysis

Hemophilia A: Intron 1 and 22 inversion mutation

Foundation for Research In Genetics and Endocrinology and Institute of Human Genetics Institute of Human Genetics
India
11
  • T Targeted variant analysis

HEMOPHILIA A

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

Hemophilia A , Deletions-Duplications (MLPA) F8 Gene

Reference Laboratory Genetics
Spain
11
  • D Deletion/duplication analysis

Hemophilia A, Sequencing F8 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 55

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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