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Results: 1 to 15 of 15
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Carrier Screening - Comprehensive Panel (145 Genes) Genesys Diagnostics Genesys Diagnostics, Inc. United States | 185 | 145 |
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DHDDS - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
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Invitae Supplemental Metabolic Newborn Screening Panel Invitae United States | 253 | 189 |
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Invitae Cerebral Palsy Spectrum Disorders Panel Invitae United States | 638 | 419 |
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Invitae Inherited Retinal Disorders Panel Invitae United States | 486 | 293 |
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Invitae Broad Carrier Screen without X-linked Disorders Invitae United States | 195 | 98 |
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Invitae United States | 224 | 112 |
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Invitae Comprehensive Carrier Screen Invitae United States | 886 | 547 |
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Invitae United States | 466 | 297 |
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Invitae Congenital Disorders of Glycosylation Panel Invitae United States | 203 | 152 |
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Comprehensive Epilepsy Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States | 234 | 240 |
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Inherited Metabolic Disorders Panel Dhiti Omics Technologies Private Ltd India | 376 | 317 |
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Developmental delay and seizures with or without movement abnormalities: Full gene sequencing CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 1 | 1 |
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Congenital Disorders of Glycolysation Asper Biogene Asper Biogene LLC Estonia | 53 | 49 |
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Institute for Human Genetics University Medical Center Freiburg Germany | 2 | 1 |
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Results: 1 to 15 of 15
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