Filters
Results: 1 to 10 of 10
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Coenzyme Q10 Deficiency NGS Panel Fulgent Genetics United States | 33 | 15 |
|
Oxidative Phosphorylation Disorders NGS Panel Fulgent Genetics United States | 416 | 235 |
|
Long QT/Brugada Syndrome NGS Panel Fulgent Genetics United States | 69 | 34 |
|
Fulgent Genetics United States | 5 | 1 |
|
Fulgent Genetics United States | 13 | 1 |
|
Catecholaminergic Polymorphic Ventricular Tachycardia NGS Panel Fulgent Genetics United States | 19 | 9 |
|
Fulgent Genetics United States | 5128 | 4672 |
|
Fulgent Genetics United States | 1103 | 676 |
|
Comprehensive Cardiovascular NGS Panel Fulgent Genetics United States | 671 | 250 |
|
Comprehensive Arrhythmia NGS Panel Fulgent Genetics United States | 184 | 76 |
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Results: 1 to 10 of 10
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.