Filters
Results: 1 to 12 of 12
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Syndromic Hearing Loss NGS Panel Fulgent Genetics United States | 223 | 83 |
|
Comprehensive Hearing Loss NGS Panel Fulgent Genetics United States | 332 | 167 |
|
Dejerine-Sottas Syndrome NGS Panel Fulgent Genetics United States | 14 | 5 |
|
Fulgent Genetics United States | 175 | 60 |
|
Paroxysmal Extreme Pain Disorder NGS Panel Fulgent Genetics United States | 185 | 53 |
|
Fulgent Genetics United States | 2 | 1 |
|
Fulgent Genetics United States | 6 | 1 |
|
Fulgent Genetics United States | 3 | 1 |
|
Fulgent Genetics United States | 7 | 1 |
|
Charcot Marie Tooth Disease Extended NGS Panel Fulgent Genetics United States | 172 | 59 |
|
Fulgent Genetics United States | 5128 | 4672 |
|
Hereditary Neuropathies NGS Panel Fulgent Genetics United States | 91 | 38 |
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Results: 1 to 12 of 12
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.