Filters

See more specimen types...
See more states

Other countries

See more countries

Results: 1 to 20 of 101 (representing 40 labs)

Tests names and labsConditionsGenes and analytesMethods

Duchenne Muscular Dystrophy

Clinical Molecular Genetics Laboratory Johns Hopkins All Children's Hospital
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Rapid microarray (CGH and SNP)

Allele Diagnostics
United States
247231
  • H Detection of homozygosity
  • D Deletion/duplication analysis
  • H Detection of homozygosity

MyoGene Panel (43 Genes)

Laboratory for Molecular Medicine Laboratory for Molecular Medicine (Partners HealthCare Personalized Medicine)
United States
10143
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Muscular dystrophy, Duchenne type

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

Pan Cardiomyopathy Panel (62 Genes)

Laboratory for Molecular Medicine Laboratory for Molecular Medicine (Partners HealthCare Personalized Medicine)
United States
10361
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

DCM/Arrhythmogenic Cardiomyopathy Panel (53 Genes)

Laboratory for Molecular Medicine Laboratory for Molecular Medicine (Partners HealthCare Personalized Medicine)
United States
9853
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Muscular dystrophy Duchenne/Becker

Human Genetics University Hospital Bern
Switzerland
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Neuromuscular Sequencing Panel

PreventionGenetics
United States
148124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

DMD. MLPA testing

Instituto de Medicina Genomica
Spain
21
  • D Deletion/duplication analysis

DMD. NextGeneDx.Complete sequencing by NGS

Instituto de Medicina Genomica
Spain
21
  • C Sequence analysis of the entire coding region

DMD. Complete sequencing

Instituto de Medicina Genomica
Spain
21
  • C Sequence analysis of the entire coding region

Dystrophinopathy via the DMD Gene

PreventionGenetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

DMD Prenatal Sequence Analysis

Baylor Genetics
United States
31
  • T Targeted variant analysis

DMD Familial Mutation/Variant Analysis

Baylor Genetics
United States
31
  • T Targeted variant analysis

DMD Deletion/Duplication Analysis - Prenatal

Baylor Genetics
United States
31
  • D Deletion/duplication analysis

DMD Deletion/Duplication Analysis

Baylor Genetics
United States
31
  • D Deletion/duplication analysis

X-chromosome High Resolution microarray analysis

Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center
United States
242171
  • D Deletion/duplication analysis

Dystrophinopathies

Molecular and Cytogenetic Diagnostic Laboratories Genetics Center
United States
22
  • D Deletion/duplication analysis

Dystrophinopathy (DMD)

Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center
United States
41
  • C Sequence analysis of the entire coding region

Rhabdomyolysis Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
7139
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 101

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.

Support Center