Filters
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 |
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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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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Molecular Genetics Laboratory London Health Sciences Centre Canada | 2 | 1 |
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Rett Syndrome exon 4 hotspot mutations Molecular Genetics Laboratory All India Institute of Medical Sciences Kalyani India | 2 | 1 |
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Centogene AG - the Rare Disease Company Germany | 5 | 1 |
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MECP2 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 5 | 1 |
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Invitae Leukodystrophy and Genetic Leukoencephalopathy Panel Invitae United States | 971 | 680 |
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Invitae Neurodevelopmental Disorders Panel Invitae United States | 404 | 241 |
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Congenital Anomalies of the Gastrointestinal Tract Panel PreventionGenetics, part of Exact Sciences United States | 297 | 180 |
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Invitae Cerebral Palsy Spectrum Disorders Panel Invitae United States | 638 | 419 |
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Autism Spectrum Disorders (ASD) Panel PreventionGenetics, part of Exact Sciences United States | 224 | 170 |
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Top 99 Genetic Causes of Developmental Delay Panel PreventionGenetics, part of Exact Sciences United States | 170 | 99 |
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Invitae Mendelian Disorders with Psychiatric Symptoms Panel Invitae United States | 247 | 163 |
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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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X-Linked Intellectual Disability Panel PreventionGenetics, part of Exact Sciences United States | 191 | 141 |
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MECP2 Sequence Analysis (Prenatal Diagnosis) Baylor Genetics United States | 6 | 1 |
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MECP2 Sequence Analysis (Familial Mutation/Variant Analysis) Baylor Genetics United States | 6 | 1 |
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