Filters
Results: 1 to 9 of 9
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Riboflavin Transporter Deficiency Neuronopathy NGS Panel Fulgent Genetics United States | 48 | 2 |
|
Syndromic Hearing Loss NGS Panel Fulgent Genetics United States | 223 | 83 |
|
Comprehensive Hearing Loss NGS Panel Fulgent Genetics United States | 332 | 167 |
|
Fulgent Genetics United States | 505 | 132 |
|
Paroxysmal Extreme Pain Disorder NGS Panel Fulgent Genetics United States | 185 | 53 |
|
Fulgent Genetics United States | 533 | 149 |
|
Fulgent Genetics United States | 29 | 1 |
|
Fulgent Genetics United States | 46 | 1 |
|
Fulgent Genetics United States | 5128 | 4672 |
|
Results: 1 to 9 of 9
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.