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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
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MEOX1 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
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Centogene AG - the Rare Disease Company Germany | 740 | 728 |
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Invitae Comprehensive Deafness Panel Invitae United States | 405 | 219 |
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Invitae Skeletal Disorders Panel Invitae United States | 624 | 349 |
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Klippel-Feil syndrome Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 5 | 5 |
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Klippel-Feil syndrome Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 5 | 5 |
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Klippel-Feil syndrome NGS panel HNL Genomics Connective Tissue Gene Tests United States | 5 | 5 |
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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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PreventionGenetics United States | 9 | 6 |
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Klippel-Feil syndrome Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 5 | 5 |
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Klippel-Feil syndrome NGS panel HNL Genomics Connective Tissue Gene Tests United States | 5 | 5 |
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Klippel-Feil syndrome Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 5 | 5 |
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Klippel-Feil Syndrome via the MEOX1 Gene PreventionGenetics United States | 1 | 1 |
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Institute for Human Genetics University Medical Center Freiburg Germany | 1 | 1 |
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Klippel-Feil syndrome: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 4 | 4 |
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Klippel-Feil Syndrome , Panel Massive Sequencing (NGS) GDF3, GDF6, MEOX1 Genes Reference Laboratory Genetics Spain | 3 | 3 |
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Laboratorio de Genetica Clinica SL Spain | 4 | 4 |
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Klippel-Feil Syndrome Type 2 , Sequencing MEOX1 Gene Reference Laboratory Genetics Spain | 1 | 1 |
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Quantitative Genomic Medicine Laboratories, SL Spain | 135 | 136 |
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