Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
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Quantitative Genomic Medicine Laboratories, SL Spain | 184 | 162 |
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Quantitative Genomic Medicine Laboratories, SL Spain | 184 | 162 |
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Quantitative Genomic Medicine Laboratories, SL Spain | 184 | 162 |
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High-Resolution Rapid Microarray (CGH and SNP) Allele Diagnostics United States | 247 | 231 |
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Rapid microarray (CGH and SNP) Allele Diagnostics United States | 247 | 231 |
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Quantitative Genomic Medicine Laboratories, SL Spain | 184 | 162 |
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SHOX gene, deletions and duplications Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS Chile | 1 | 1 |
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Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS Chile | 1 | 1 |
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Centogene AG - the Rare Disease Company Germany | 3 | 1 |
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Centogene AG - the Rare Disease Company Germany | 3 | 1 |
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Leri-Weill dyschondrosteosis, 127300, Autosomal dominant; LWD (Léri-Weill dyschondrosteosis) (MLPA) 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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Quantitative Genomic Medicine Laboratories, SL Spain | 184 | 162 |
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Leri-Weill dyschondrosteosis Comprehensive Test HNL Genomics Connective Tissue Gene Tests United States | 1 | 1 |
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Leri-Weill dyschondrosteosis Sequencing Test HNL Genomics Connective Tissue Gene Tests United States | 1 | 1 |
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Leri-Weill dyschondrosteosis Deletion / Duplication Test HNL Genomics Connective Tissue Gene Tests United States | 1 | 1 |
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X-chromosome High Resolution microarray analysis Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center United States | 240 | 171 |
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Short stature Homeobox (SHOX)-related Haploinsufficiency Disorder via the SHOX Gene PreventionGenetics, part of Exact Sciences United States | 3 | 1 |
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MNG Laboratories (Medical Neurogenetics, LLC.) United States | 3 | 1 |
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Institute for Human Genetics University Medical Center Freiburg Germany | 3 | 1 |
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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.