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Results: 1 to 16 of 16
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
EPHX2 Gene Hypercholesterolemia, familial, due to LDLR defect, modifier of NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 195 | 221 |
|
EPHX2 - 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 | 669 | 688 |
|
Centogene AG - the Rare Disease Company Germany | 406 | 414 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Translational Metabolic Laboratory Radboud University Medical Centre Netherlands | 1 | 625 |
|
Dyslipidemia (WES based NGS panel of 25 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 25 |
|
CGC Genetics Unilabs Portugal | 1 | 26 |
|
MITOCHONDRIAL DISEASES PANEL (NUCLEAR GENES) Laboratorio de Genetica Clinica SL Spain | 1 | 1372 |
|
Inherited Metabolic Disorders Panel Dhiti Omics Technologies Private Ltd India | 376 | 317 |
|
Familial hypercholesterolemia panel. 16-gene NGS panel. Genologica Medica Spain | 20 | 16 |
|
Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
|
Fulgent Genetics United States | 1 | 1 |
|
Fulgent Genetics United States | 5129 | 4672 |
|
Results: 1 to 16 of 16
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