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Results: 81 to 92 of 92

Tests names and labsConditionsGenes, analytes, and microbesMethods

XLID (X-Linked Intellectual Disability) NGS Panel

Fulgent Genetics
United States
162117
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Duchenne or Becker Muscular Dystrophy (DMD/BMD)

Center for Human Genetics, Inc
United States
21
  • D Deletion/duplication analysis

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

Autism NGS Panel

Fulgent Genetics
United States
170106
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Dystrophinopathies

Molecular Genetics Laboratory BC Children's and BC Women's Hospitals
Canada
41
  • D Deletion/duplication analysis

Muscular dystrophy Becker

MedGene
Slovakia
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cardiovascular NGS Panel

Fulgent Genetics
United States
671250
  • 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 Becker

Praxis fuer Humangenetik Wien
Austria
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Duchenne and Becker Muscular Dystrophy

Molecular Genetics Laboratory - Diagnostics Genetics LabPLUS - Auckland City Hospital
New Zealand
31
  • D Deletion/duplication analysis

Dystrophinopathies

Institute of Medical Genetics and Genomics Sir Ganga Ram Hospital
India
31
  • D Deletion/duplication analysis
  • L Linkage analysis
  • E Sequence analysis of select exons

Results: 81 to 92 of 92

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.