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Results: 1 to 14 of 14
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Trichorhinophalangeal syndrome type I (sequence analysis of TRPS1 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Optic Atrophy and Neuropathy Panel PreventionGenetics, part of Exact Sciences United States | 96 | 68 |
|
Hereditary Spastic Paraplegia Panel CGC Genetics Unilabs Portugal | 1 | 97 |
|
Mendelics Brazil | 1 | 104 |
|
Codex Genetics Limited Hong Kong | 1 | 490 |
|
Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
|
Xpanded Adult Movement Disorders Panel GeneDx United States | 5 | 473 |
|
GeneDx United States | 2 | 2592 |
|
GeneDx United States | 1 | 999 |
|
Neuromuscular disorders - different panels Institute of Human Genetics Cologne University Germany | 16 | 474 |
|
Hereditary Spastic Paraplegia NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 81 | 79 |
|
Mental retardation - different panels Institute of Human Genetics Cologne University Germany | 7 | 2536 |
|
Fulgent Genetics United States | 1 | 1 |
|
Results: 1 to 14 of 14
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.