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Results: 1 to 20 of 20
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
SNAI2 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
|
Invitae Hypopigmentation Panel Invitae United States | 83 | 46 |
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Invitae Comprehensive Deafness Panel Invitae United States | 405 | 219 |
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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 |
|
Hereditary Hearing Loss and Deafness Panel PreventionGenetics, part of Exact Sciences United States | 360 | 222 |
|
PreventionGenetics, part of Exact Sciences United States | 39 | 33 |
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Waardenburg syndrome Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 8 | 7 |
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Waardenburg syndrome Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 8 | 7 |
|
PreventionGenetics, part of Exact Sciences United States | 12 | 6 |
|
Waardenburg Syndrome Type IID via the SNAI2 Gene PreventionGenetics, part of Exact Sciences United States | 2 | 1 |
|
Syndromic Hearing Loss NGS Panel Fulgent Genetics United States | 223 | 83 |
|
Comprehensive Hearing Loss NGS Panel Fulgent Genetics United States | 332 | 167 |
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Hearing Loss Advanced Sequencing and CNV Evaluation Athena Diagnostics Inc United States | 249 | 184 |
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Laboratorio de Genetica Clinica SL Spain | 4 | 4 |
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Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 9 | 6 |
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Fulgent Genetics United States | 2 | 1 |
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Fulgent Genetics United States | 5129 | 4672 |
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Waardenburg Syndrome NGS Panel Fulgent Genetics United States | 19 | 6 |
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Fulgent Genetics United States | 52 | 28 |
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Results: 1 to 20 of 20
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