U.S. flag

An official website of the United States government

Filters

See more specimen types...

Other countries

See more countries

Results: 41 to 58 of 58

Tests names and labsConditionsGenes, analytes, and microbesMethods

Comprehensive Primary Immunodeficiency NGS Panel

Fulgent Genetics
United States
1048472
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Thrombosis, Platelet Disorder, and Coagulation Deficiency NGS Panel

Fulgent Genetics
United States
14682
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Afibrinogenemia NGS Panel

Fulgent Genetics
United States
133
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Coagulation Disorders

Asper Biogene Asper Biogene LLC
Estonia
2116
  • C Sequence analysis of the entire coding region

AFIBRINOGENEMIA – DYSFIBRINOGENEMIA – HYPOFIBRINOGENEMIA

Laboratorio de Genetica Clinica SL
Spain
23
  • C Sequence analysis of the entire coding region

Afibrinogenemia, congenital

Labor Dr. Wisplinghoff
Germany
13
  • C Sequence analysis of the entire coding region

Comprehensive Hematology Panel

Blueprint Genetics
Finland
4239
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

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

Platelet Disorders

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
1255
  • C Sequence analysis of the entire coding region

FGB Single Gene

Fulgent Genetics
United States
121
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Afibrinogenemia, congenital

Bioarray
Spain
11
  • 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

Clinical Exome

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

Dysfibrinogenemia

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Afibrinogenemia, congenital

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Dysfibrinogenemia

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Afibrinogenemia, congenital

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Results: 41 to 58 of 58

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.