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Results: 21 to 28 of 28

Tests names and labsConditionsGenes, analytes, and microbesMethods

Dejerine-Sottas Syndrome NGS Panel

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

Paroxysmal Extreme Pain Disorder NGS Panel

Fulgent Genetics
United States
18553
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Peripheral Neuropathy , Panel Massive Sequencing (NGS) 31 Genes

Reference Laboratory Genetics
Spain
4131
  • C Sequence analysis of the entire coding region

Single gene testing PMP22

CeGaT GmbH
Germany
61
  • C Sequence analysis of the entire coding region

PMP22 Single Gene

Fulgent Genetics
United States
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Charcot Marie Tooth Disease Extended NGS Panel

Fulgent Genetics
United States
17259
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51274672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Neuropathies NGS Panel

Fulgent Genetics
United States
9138
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 28 of 28

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.