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Results: 81 to 90 of 90

Tests names and labsConditionsGenes, analytes, and microbesMethods

Congenital Myasthenic Syndromes and Arthrogryposis Panel

CeGaT GmbH
Germany
944
  • C Sequence analysis of the entire coding region

OI panel 2

Connective Tissue Laboratory Ghent University Hospital
Belgium
119
  • C Sequence analysis of the entire coding region

PLOD2 mutational analysis

Connective Tissue Laboratory Ghent University Hospital
Belgium
11
  • E Sequence analysis of select exons

PLOD2 Single Gene

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

Skeletal Dysplasias NGS Panel

Fulgent Genetics
United States
543178
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasia

Asper Biogene Asper Biogene LLC
Estonia
16674
  • 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

Bruck syndrome 2

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

Bruck syndrome 2

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

Osteogenesis Imperfecta

Amplexa Genetics Amplexa Genetics A/S
Denmark
115
  • C Sequence analysis of the entire coding region

Results: 81 to 90 of 90

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.