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Results: 21 to 29 of 29

Tests names and labsConditionsGenes, analytes, and microbesMethods

Myasthenic syndrome, congenital: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
3125
  • C Sequence analysis of the entire coding region

Arthrogryposis NGS Panel

Fulgent Genetics
United States
17560
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Myasthenic Syndrome

Asper Biogene Asper Biogene LLC
Estonia
4623
  • C Sequence analysis of the entire coding region

Congenital Myasthenia , Panel Massive Sequencing (NGS) 12 Genes

Reference Laboratory Genetics
Spain
1812
  • C Sequence analysis of the entire coding region

Congenital Myasthenic Syndrome Advanced Sequencing Evaluation

Athena Diagnostics
United States
1713
  • C Sequence analysis of the entire coding region

Congenital myasthenic syndrome

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

AGRN Single Gene

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

Congenital Myasthenic Syndrome NGS Panel

Fulgent Genetics
United States
10528
  • 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

Results: 21 to 29 of 29

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.