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Results: 61 to 74 of 74

Tests names and labsConditionsGenes, analytes, and microbesMethods

GP1BB Single Gene

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

GP1BA Single Gene

Fulgent Genetics
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

GP9 Single Gene

Fulgent Genetics
United States
11
  • 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

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Thrombocytopenia NGS Panel

Fulgent Genetics
United States
3215
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bernard-Soulier syndrome C

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

Bernard-Soulier syndrome B

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

Bernard-Soulier syndrome A1

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

Bernard-Soulier syndrome B

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

Bernard-Soulier syndrome C

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

Bernard-Soulier syndrome A1

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

Bernard Soulier Syndrome

Institute of Human Genetics Universitätsmedizin Greifswald
Germany
43
  • C Sequence analysis of the entire coding region

Bernard -Soulier Syndrome

Genetics Laboratory University of Oklahoma Health Sciences Center
United States
13
  • C Sequence analysis of the entire coding region

Results: 61 to 74 of 74

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.