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Results: 61 to 75 of 75

Tests names and labsConditionsGenes, analytes, and microbesMethods

Epilepsy Comprehensive NGS Panel

Fulgent Genetics
United States
729398
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Walker-Warburg Syndrome Panel

CeGaT GmbH
Germany
215
  • C Sequence analysis of the entire coding region

POMGNT1 Single Gene

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Syndromic Congenital Muscular Dystrophy NGS Panel

Fulgent Genetics
United States
145
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Dystroglycan-Related Congenital Muscular Dystrophy NGS Panel

Fulgent Genetics
United States
6713
  • 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

Neuromuscular NGS Panel

Fulgent Genetics
United States
259112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1058554
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Lissencephaly NGS Panel

Fulgent Genetics
United States
3114
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Muscular dystrophy / dystroglycanopathy A3

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

Comprehensive Eye Disorders NGS Panel

Fulgent Genetics
United States
1018459
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Muscular Dystrophies NGS Panel

Fulgent Genetics
United States
12542
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Muscular dystrophy / dystroglycanopathy A3

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

Test for POMGNT1-Related Muscle Diseases

Genome Diagnostics Laboratory Hospital For Sick Children
Canada
11
  • E Enzyme assay
  • C Sequence analysis of the entire coding region

Results: 61 to 75 of 75

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.