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Results: 1 to 12 of 12
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Hypercholesterolemia, familial (sequence analysis of PCSK9 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 243 | 238 |
|
TTC12 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 289 | 275 |
|
Primary Ciliary Dyskinesia (PCD) via the TTC12 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
Heterotaxy, Situs Inversus and Kartagener's Syndrome Panel PreventionGenetics, part of Exact Sciences United States | 43 | 48 |
|
Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins University, School of Medicine United States | 162 | 129 |
|
Primary Ciliary Dyskinesia (PCD)/Immotile Cilia Syndrome Panel PreventionGenetics, part of Exact Sciences United States | 44 | 50 |
|
PreventionGenetics, part of Exact Sciences United States | 135 | 133 |
|
Primary Ciliary Dyskinesia (PCD)/Immotile Cilia Syndrome and Cystic Fibrosis Panel PreventionGenetics, part of Exact Sciences United States | 44 | 51 |
|
CGC Genetics Unilabs Portugal | 1 | 184 |
|
Fulgent Genetics United States | 1 | 1 |
|
Results: 1 to 12 of 12
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