Filters
Results: 1 to 17 of 17
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Retinopathy and Optic Atrophy NGS Panel Fulgent Genetics United States | 563 | 241 |
|
Paroxysmal Extreme Pain Disorder NGS Panel Fulgent Genetics United States | 185 | 53 |
|
Oxidative Phosphorylation Disorders NGS Panel Fulgent Genetics United States | 416 | 235 |
|
Fulgent Genetics United States | 9 | 1 |
|
Fulgent Genetics United States | 15 | 1 |
|
Fulgent Genetics United States | 19 | 1 |
|
Fulgent Genetics United States | 12 | 1 |
|
Fulgent Genetics United States | 22 | 1 |
|
Fulgent Genetics United States | 19 | 1 |
|
Fulgent Genetics United States | 19 | 1 |
|
Fulgent Genetics United States | 8 | 1 |
|
Fulgent Genetics United States | 11 | 1 |
|
Fulgent Genetics United States | 9 | 1 |
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Charcot Marie Tooth Disease Extended NGS Panel Fulgent Genetics United States | 172 | 59 |
|
Fulgent Genetics United States | 5128 | 4672 |
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Fulgent Genetics United States | 1103 | 676 |
|
Comprehensive Eye Disorders NGS Panel Fulgent Genetics United States | 1018 | 459 |
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Results: 1 to 17 of 17
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.