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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Labcorp Genetics (formerly Invitae) LabCorp United States | 24 | 8 |
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F2 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 4 | 1 |
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Stroke, Cerebral Hemorrhage, Hemiplegia, and Migraine Panel PreventionGenetics, part of Exact Sciences United States | 346 | 160 |
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Labcorp Genetics (formerly Invitae) LabCorp United States | 409 | 164 |
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Labcorp Genetics (formerly Invitae) LabCorp United States | 208 | 81 |
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Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins University, School of Medicine United States | 525 | 338 |
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Hemophilia: Factor II and Factor V gene mutation study Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 2 | 2 |
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Quantitative Genomic Medicine Laboratories, SL Spain | 327 | 300 |
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Invitae Hereditary Thrombophilia Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 24 | 11 |
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PreventionGenetics, part of Exact Sciences United States | 78 | 79 |
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Molecular Haemostasis & Thrombosis Synnovis Analytics LLP - Guy's and St. Thomas' NHS Foundation Trust United Kingdom | 1 | 1 |
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Prothrombin/Factor II Deficiency via the F2 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
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Coagulation Factor Deficiency Panel PreventionGenetics, part of Exact Sciences United States | 21 | 20 |
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Baylor Genetics United States | 11 | 3 |
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Baylor Genetics United States | 4 | 1 |
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Clotting factor deficiency panel. 16-gene NGS panel. Genologica Medica Spain | 29 | 16 |
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Bleeding disorder / coagulopathy panel. NGS panel of 62 genes. Genologica Medica Spain | 96 | 62 |
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Factor II (prothrombin) mutation analysis Genetiks Genetic Diagnosis Center Genetic Diseases Evaluation Center Turkey | 1 | 1 |
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