Filters
Results: 1 to 15 of 15
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 |
|
Fulgent Genetics United States | 186 | 61 |
|
Comprehensive Primary Immunodeficiency NGS Panel Fulgent Genetics United States | 1048 | 472 |
|
Paroxysmal Extreme Pain Disorder NGS Panel Fulgent Genetics United States | 185 | 53 |
|
Fulgent Genetics United States | 533 | 149 |
|
Fulgent Genetics United States | 46 | 1 |
|
Fulgent Genetics United States | 16 | 1 |
|
Fulgent Genetics United States | 11 | 1 |
|
Fulgent Genetics United States | 5128 | 4672 |
|
Fulgent Genetics United States | 94 | 31 |
|
Amyotrophic Lateral Sclerosis NGS Panel Fulgent Genetics United States | 84 | 43 |
|
Comprehensive Eye Disorders NGS Panel Fulgent Genetics United States | 1018 | 459 |
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Results: 1 to 15 of 15
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.