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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
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Branchiootorenal Syndrome Panel CeGaT GmbH Germany | 4 | 4 |
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SIX1-Related Branchiootorenal Spectrum Disorders Bioscientia GmbH Center for Human Genetics Germany | 1 | 1 |
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SIX1 Deletion/duplication analysis Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 2 | 1 |
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Fulgent Genetics United States | 3 | 1 |
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Fulgent Genetics United States | 5129 | 4672 |
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Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 2 | 1 |
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Branchiootorenal Spectrum Disorder Panel Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 5 | 3 |
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OtoSeq Hearing Loss Panel by next-generation sequencing (NGS) Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 36 | 23 |
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IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.