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Results: 1 to 20 of 95 (representing 36 labs)

Tests names and labsConditionsGenes and analytesMethods

AllNeuro panel

Centogene AG - the Rare Disease Company
Germany
6021038
  • C Sequence analysis of the entire coding region

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

MyoGene Panel (43 Genes)

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, Becker 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 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 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

qCarrier Plus

Quantitative Genomic Medicine Laboratories, SL
Spain
329300
  • -- Sequence analysis of the entire coding region

Comprehensive Neuromuscular NextGen Sequencing (NGS) 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

Dystrophinopathy (DMD)

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

DMD Evaluation

Athena Diagnostics Inc
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 95

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.

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