Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Myotonic dystrophy: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 2 | 2 |
|
Myotonic Dystrophy Type 1 (DMPK) Repeat Expansion Fulgent Genetics United States | 1 | 1 |
|
Genetics Service Unit National Institute of Biomedical Genomics India | 1 | 1 |
|
CHEO Genetics Diagnostic Laboratory Children's Hospital of Eastern Ontario Canada | 1 | 1 |
|
MYOTONIC DYSTROPHY TYPE 1 (STEINERT) Laboratorio de Genetica Clinica SL Spain | 1 | 1 |
|
Steinert myotonic dystrophy syndrome Labor Dr. Wisplinghoff Germany | 1 | 1 |
|
Myotonic Syndrome Advanced Evaluation Athena Diagnostics United States | 9 | 7 |
|
Myotonic Dystrophy Type 1 - DMPK Gene Center for Comprehensive Genetic Services Shahid Beheshti University of Medical Sciences Iran | 1 | 1 |
|
Myotonic dystrophy type I mutation analysis Diagnostics Division CENTRE FOR DNA FINGERPRINTING AND DIAGNOSTICS India | 1 | 1 |
|
Bioarray Spain | 1 | 1 |
|
CeGaT GmbH Germany | 37 | 32 |
|
MVZ Dr. Eberhard & Partner Dortmund Germany | 1 | 1 |
|
MVZ Dr. Eberhard & Partner Dortmund Germany | 1 | 1 |
|
Fulgent Genetics United States | 1 | 1 |
|
Early Onset Myotonia Evaluation Athena Diagnostics United States | 4 | 3 |
|
Athena Diagnostics United States | 1 | 1 |
|
Myotonic Dystrophy Type 1 - DMPK Gene Genomic Research Center Shahid Beheshti University of Medical Sciences Iran | 1 | 1 |
|
Myotonic Dystrophy Type 1 Repeat Expansion Analysis (Prenatal Diagnosis) Baylor Genetics United States | 1 | 1 |
|
Fulgent Genetics United States | 5128 | 4672 |
|
Praxis fuer Humangenetik Wien Austria | 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.