Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Myotonic Dystrophy - DMPK Gene Center for Genetics at Saint Francis Saint Francis Hospital United States | 1 | 1 |
|
Genetics Laboratory Shodair Children's Hospital United States | 1 | 1 |
|
GENETIX Centro de Investigación en Genética Humana y Reproductiva Colombia | 1 | 1 |
|
Myotonic Dystrophy type 1 (DMPK gene) Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS Chile | 1 | 1 |
|
Diagnostic génotypique direct de la dystrophie myotonique de Steinert (Gène DM) Laboratoire de Diagnostic Moleculaire Hopital Saint-Francois d'Assise du CHU de Québec UL Canada | 1 | 1 |
|
Dystrophia myotonica protein kinase (DMPK) gene CTG triplet repeat test Neurogenetics Department Cyprus Institute of Neurology and Genetics Cyprus | 1 | 1 |
|
DMPK - NGS including CNV analysis Centogene US, LLC - The Rare Disease Company United States | 1 | 1 |
|
Centogene US, LLC - The Rare Disease Company United States | 325 | 316 |
|
Centogene US, LLC - The Rare Disease Company United States | 1886 | 1858 |
|
DMPK - Repeat expansion analysis Centogene US, LLC - The Rare Disease Company United States | 1 | 1 |
|
DMPK - Repeat expansion analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
DMPK - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
|
Centogene AG - the Rare Disease Company Germany | 325 | 316 |
|
Myotonic dystrophy 1, 160900, Autosomal dominant; DM1 (Steinert myotonic dystrophy)(Repeat Analysis) Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
|
Genomic Unity Neuromuscular Disorders Analysis (includes CNBP, DMPK STR analysis) Variantyx, Inc. United States | 5 | 3 |
|
IU Genetic Testing Laboratories Indiana University School of Medicine United States | 1 | 1 |
|
Myotonic Dystrophy Type 1 Repeat Expansion Analysis (Prenatal Diagnosis) Baylor Genetics United States | 1 | 1 |
|
Myotonic Dystrophy Type 1 Repeat Expansion Analysis Baylor Genetics United States | 1 | 1 |
|
Molecular Diagnostic Laboratory Diagnostic Services, Shared Health Manitoba Canada | 1 | 1 |
|
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.