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Results: 1 to 15 of 15
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
POMGNT2 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
|
Invitae Rhabdomyolysis and Metabolic Myopathy Panel Invitae United States | 202 | 128 |
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Invitae Supplemental Metabolic Newborn Screening Panel Invitae United States | 253 | 189 |
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Invitae Brain Malformations Panel Invitae United States | 247 | 161 |
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Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins Hospital United States | 480 | 254 |
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Invitae Congenital Muscular Dystrophy Panel Invitae United States | 64 | 28 |
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Invitae Comprehensive Muscular Dystrophy Panel Invitae United States | 114 | 52 |
|
Invitae Congenital Disorders of Glycosylation Panel Invitae United States | 203 | 152 |
|
Invitae Limb-Girdle Muscular Dystrophy Panel Invitae United States | 91 | 37 |
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Invitae Comprehensive Neuromuscular Disorders Panel Invitae United States | 353 | 208 |
|
Asper Biogene Asper Biogene LLC Estonia | 59 | 28 |
|
Muscular dystrophy, limb-girdle, autosomal recessive: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 27 | 29 |
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Muscular dystrophy-dystroglycanopathy, type C: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 10 | 10 |
|
Limb-Girdle Muscular Dystrophy Asper Biogene Asper Biogene LLC Estonia | 87 | 39 |
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Results: 1 to 15 of 15
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.