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Results: 1 to 20 of 51

Tests names and labsConditionsGenes, analytes, and microbesMethods

Myotonic Dystrophy - DMPK Gene

Center for Genetics at Saint Francis Saint Francis Hospital
United States
11
  • T Targeted variant analysis

Myotonic Dystrophy

Genetics Laboratory Shodair Children's Hospital
United States
11
  • T Targeted variant analysis

Myotonic Dystrophy Type 1

GENETIX Centro de Investigación en Genética Humana y Reproductiva
Colombia
11
  • T Targeted variant analysis

Myotonic Dystrophy type 1 (DMPK gene)

Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS
Chile
11
  • T Targeted variant analysis

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
11
  • T Targeted variant analysis

Dystrophia myotonica protein kinase (DMPK) gene CTG triplet repeat test

Neurogenetics Department Cyprus Institute of Neurology and Genetics
Cyprus
11
  • T Targeted variant analysis

DMPK - Repeat expansion analysis

Centogene AG - the Rare Disease Company
Germany
11
  • T Targeted variant analysis

DMPK - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CentoNeuro Panel

Centogene AG - the Rare Disease Company
Germany
18861858
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neuromuscular Panel

Centogene AG - the Rare Disease Company
Germany
325316
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Myotonic dystrophy 1, 160900, Autosomal dominant; DM1 (Steinert myotonic dystrophy)(Repeat Analysis)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • T Targeted variant analysis

Genomic Unity Neuromuscular Disorders Analysis (includes STR analysis of CNBP, DMPK, GIPC1, LRP12, RFC1 and VWA1 genes).

Variantyx, Inc.
United States
53
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Myotonic Dystrophy (PCR only)

IU Genetic Testing Laboratories Indiana University School of Medicine
United States
11
  • T Targeted variant analysis

Myotonic Dystrophy Type 1 Repeat Expansion Analysis (Prenatal Diagnosis)

Baylor Genetics
United States
11
  • T Targeted variant analysis

Myotonic Dystrophy Type 1 Repeat Expansion Analysis

Baylor Genetics
United States
11
  • T Targeted variant analysis

myotonic dystrophy type 1

Molecular Diagnostic Laboratory Diagnostic Services, Shared Health Manitoba
Canada
11
  • T Targeted variant analysis

Myotonic dystrophy type I (Steinert disease, DM1, CTG expansion on DMPK gene)

CGC Genetics Unilabs
Portugal
11
  • T Targeted variant analysis

Skeletal diseases. NGS panel of 169 genes.

Genologica Medica
Spain
373169
  • C Sequence analysis of the entire coding region

Myotonic Dystrophy

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • T Targeted variant analysis

Myotonic Dystrophy 1 (DMPK) Genetic Testing (Repeat Expansion)

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
11
  • E Sequence analysis of select exons

Results: 1 to 20 of 51

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.