Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Comprehensive Cardiovascular NGS Panel Fulgent Genetics United States | 671 | 250 |
|
Marfan Syndrome and Thoracic Aortic Aneurysm and Dissection NGS Panel Fulgent Genetics United States | 65 | 31 |
|
Weill-Marchesani syndrome 2, dominant Praxis fuer Humangenetik Wien Austria | 1 | 1 |
|
Marfan Syndrome and MFS Related Disorders Panel Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 7 | 3 |
|
FBN1 sequencing and deletion/duplication analysis Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center Netherlands | 4 | 1 |
|
Marfan Syndrome (FBN1) Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States | 8 | 1 |
|
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.