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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Molecular Vision Laboratory United States | 1358 | 1028 |
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CIB2 - NGS including CNV analysis Centogene US, LLC - The Rare Disease Company United States | 2 | 1 |
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Centogene US, LLC - The Rare Disease Company United States | 203 | 194 |
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Centogene US, LLC - The Rare Disease Company United States | 417 | 413 |
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Centogene US, LLC - The Rare Disease Company United States | 1886 | 1858 |
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Centogene US, LLC - The Rare Disease Company United States | 777 | 770 |
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CIB2 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
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Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
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Centogene AG - the Rare Disease Company Germany | 777 | 770 |
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Centogene AG - the Rare Disease Company Germany | 417 | 413 |
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Centogene AG - the Rare Disease Company Germany | 203 | 194 |
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Invitae Comprehensive Deafness Panel Invitae United States | 405 | 219 |
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Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics United States | 288 | 218 |
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Invitae United States | 32 | 17 |
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Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
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Invitae Inherited Retinal Disorders Panel Invitae United States | 486 | 293 |
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Hereditary Hearing Loss and Deafness Panel PreventionGenetics United States | 356 | 209 |
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Molecular Vision Laboratory United States | 342 | 268 |
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Usher Syndrome Type IJ and Deafness, Autosomal Recessive 48 (DFNB48) via the CIB2 Gene PreventionGenetics United States | 2 | 1 |
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Non-syndromic hearing loss panel. 95-gene NGS panel. Genologica Medica Spain | 146 | 94 |
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