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Results: 1 to 11 of 11
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
EPB41 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Bone Marrow Failure / Anemia Panel Centogene AG - the Rare Disease Company Germany | 212 | 212 |
|
Invitae Red Blood Cell Membrane Disorders and Enzymopathies Panel Invitae United States | 57 | 28 |
|
Invitae Hereditary Hemolytic Anemia Panel Invitae United States | 74 | 39 |
|
Hereditary Hemolytic Anemia Panel PreventionGenetics, part of Exact Sciences United States | 44 | 34 |
|
Spherocytosis/Elliptocytosis Panel PreventionGenetics, part of Exact Sciences United States | 8 | 6 |
|
Fulgent Genetics United States | 61 | 24 |
|
EPB41 Deletion/duplication analysis Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 1 | 1 |
|
Fulgent Genetics United States | 1 | 1 |
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Fulgent Genetics United States | 5124 | 4672 |
|
Erythrocyte membrane disorder panel Genome Diagnostics Laboratory University Medical Center Utrecht Netherlands | 16 | 7 |
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Results: 1 to 11 of 11
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.