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Results: 1 to 13 of 13
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
SASH1 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
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Centogene AG - the Rare Disease Company Germany | 777 | 770 |
|
CGC Genetics Unilabs Portugal | 1 | 34 |
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CGC Genetics Unilabs Portugal | 1 | 277 |
|
Hereditary Cancer Panel (Complete) Mendelics Brazil | 1 | 264 |
|
Cancer, alopecia, pigment dyscrasia, onychodystrophy, and keratoderma: Full gene sequencing CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 1 | 1 |
|
Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
|
Prenatal Known Familial Mutation GeneDx United States | 1 | 1716 |
|
Custom XomeDxSlice (2-150 Genes, Proband Only) GeneDx United States | 1 | 1718 |
|
Dyschromatosis universalis hereditaria: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 2 | 2 |
|
Dyschromatosis universalis hereditaria Laboratorio de Genetica Clinica SL Spain | 1 | 2 |
|
Fulgent Genetics United States | 5 | 1 |
|
Results: 1 to 13 of 13
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