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Results: 1 to 20 of 20
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
TMTC3 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
|
Centogene AG - the Rare Disease Company Germany | 777 | 770 |
|
Centogene AG - the Rare Disease Company Germany | 740 | 728 |
|
Invitae Leukodystrophy and Genetic Leukoencephalopathy Panel Invitae United States | 971 | 680 |
|
Invitae Brain Malformations Panel Invitae United States | 247 | 161 |
|
PreventionGenetics, part of Exact Sciences United States | 29 | 28 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
PreventionGenetics, part of Exact Sciences United States | 79 | 52 |
|
HNL Genomics Connective Tissue Gene Tests United States | 11 | 10 |
|
Lissencephaly core Comprehensive test HNL Genomics Connective Tissue Gene Tests United States | 11 | 10 |
|
Lissencephaly core Deletion / Duplication test HNL Genomics Connective Tissue Gene Tests United States | 11 | 10 |
|
Lissencephaly and related disorders Comprehensive test HNL Genomics Connective Tissue Gene Tests United States | 46 | 42 |
|
Lissencephaly and related disorders Deletion / Duplication test HNL Genomics Connective Tissue Gene Tests United States | 46 | 42 |
|
Lissencephaly and related disorders NGS test HNL Genomics Connective Tissue Gene Tests United States | 46 | 42 |
|
Comprehensive Brain Malformation Panel Genetic Services Laboratory University of Chicago United States | 37 | 131 |
|
Institute for Human Genetics University Medical Center Freiburg Germany | 1 | 1 |
|
Comprehensive Brain Malformations Panel GeneDx United States | 19 | 103 |
|
Lissencephaly: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 14 | 11 |
|
Results: 1 to 20 of 20
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.