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Results: 1 to 16 of 16
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
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Centogene AG - the Rare Disease Company Germany | 734 | 744 |
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Centogene AG - the Rare Disease Company Germany | 777 | 770 |
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Centogene AG - the Rare Disease Company Germany | 669 | 688 |
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Centogene AG - the Rare Disease Company Germany | 829 | 848 |
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Invitae Brain Malformations Panel Invitae United States | 247 | 161 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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MNG Laboratories (Medical Neurogenetics, LLC.) United States | 414 | 800 |
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Polymicrogyria panel. 17-gene NGS panel. Genologica Medica Spain | 22 | 17 |
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Neuronal migration disorder panel. NGS panel of 58 genes. Genologica Medica Spain | 110 | 57 |
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Brain Malformations Panel, Comprehensive CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 111 | 56 |
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Pseudo-TORCH syndrome: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 2 | 2 |
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Malformations of Cortical Development , Panel Massive Sequencing (NGS) 38 Genes Reference Laboratory Genetics Spain | 41 | 38 |
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Polymicrogyria , Panel Massive Sequencing (NGS) 10 Genes Reference Laboratory Genetics Spain | 11 | 10 |
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PSEUDO-TORCH SYNDROME (BARAITSER-BRETT-PIESOWICZ SYNDROME) Laboratorio de Genetica Clinica SL Spain | 1 | 1 |
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Results: 1 to 16 of 16
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