Filters
Results: 1 to 12 of 12
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Comprehensive Primary Immunodeficiency NGS Panel Fulgent Genetics United States | 1048 | 472 |
|
Comprehensive Cardiomyopathy NGS Panel Fulgent Genetics United States | 450 | 128 |
|
Neuronal Migration Disorders NGS Panel Fulgent Genetics United States | 392 | 83 |
|
Noonan and RASopathies NGS Panel Fulgent Genetics United States | 235 | 26 |
|
Congenital Heart Defect NGS Panel Fulgent Genetics United States | 377 | 114 |
|
Cerebral Cortical Malformation NGS Panel Fulgent Genetics United States | 210 | 42 |
|
Fulgent Genetics United States | 178 | 1 |
|
Fulgent Genetics United States | 49 | 1 |
|
Hypertrophic Cardiomyopathy NGS Panel Fulgent Genetics United States | 375 | 86 |
|
Congenital Myasthenic Syndrome NGS Panel Fulgent Genetics United States | 105 | 28 |
|
Fulgent Genetics United States | 5128 | 4672 |
|
Comprehensive Cardiovascular NGS Panel Fulgent Genetics United States | 671 | 250 |
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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.