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Results: 1 to 15 of 15
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Congenital Adrenal Hyperplasia (CAH) Panel Centogene AG - the Rare Disease Company Germany | 12 | 12 |
|
Centogene AG - the Rare Disease Company Germany | 247 | 262 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Primary Pigmented Nodular Adrenocortical Disease via the PDE11A Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
Primary pigmented nodular adrenocortical disease type 2 (sequence analysis of PDE11A gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Laboratorio de Genetica Clinica SL Spain | 1 | 249 |
|
Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
|
Comprehensive Dementia (NGS Panel and Copy Number Analysis) MNG Laboratories (Medical Neurogenetics, LLC.) United States | 10 | 145 |
|
Prenatal Known Familial Mutation GeneDx United States | 1 | 1716 |
|
Custom XomeDxSlice (2-150 Genes, Proband Only) GeneDx United States | 1 | 1718 |
|
Pigmented nodular adrenocortical disease, primary: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 4 | 4 |
|
CEN4GEN Comprehensive Hereditary Cancer Syndrome: Gene sequencing Panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 1 | 143 |
|
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2; PPNAD2 Bioarray Spain | 1 | 1 |
|
Fulgent Genetics United States | 1 | 1 |
|
Fulgent Genetics United States | 5128 | 4672 |
|
Results: 1 to 15 of 15
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