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Results: 1 to 20 of 50

Tests names and labsConditionsGenes and analytesMethods

AllNeuro panel

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

Limb-Girdle Muscular Dystrophy Sequencing Panel

Genetic Services Laboratory University of Chicago
United States
4630
  • C Sequence analysis of the entire coding region

Limb-Girdle Muscular Dystrophy Deletion/Duplication Panel

Genetic Services Laboratory University of Chicago
United States
3925
  • D Deletion/duplication analysis

Myofibrillar Myopathy Panel (8 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
208
  • 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
9543
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Muscular Dystrophy (LGMD/EDMD) Panel (25 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
6425
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Limb-girdle muscular dystrophy, autosomal dominant type 1A

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

MYOT. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

TruGenome Predisposition Screen (Whole Genome Sequencing)

Illumina Clinical Services Laboratory Illumina
United States
15411578
  • C Sequence analysis of the entire coding region

TTID. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

Limb-Girdle Muscular Dystrophy (LGMD) NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
2224
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Distal Hereditary Myopathy NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
2018
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Autosomal Dominant Limb-Girdle Muscular Dystrophy (LGMD) Sequencing Panel

PreventionGenetics
United States
77
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Myotilinopathy Testing via the MYOT Gene

PreventionGenetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

LIMB-GIRDLE MUSCULAR DYSTROPHY, A.D.

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
55
  • C Sequence analysis of the entire coding region

LIMB-GIRDLE MUSCULAR DYSTROPHY

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
2722
  • C Sequence analysis of the entire coding region

Neuromuscular Disorders Sequencing Panel

Genetic Services Laboratory University of Chicago
United States
9988
  • C Sequence analysis of the entire coding region

Autosomal dominant limb-girdle muscular dystrophy type 1A

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Limb-girdle muscular dystrophy type 1A (LGMD1A, sequence analysis of MYOT gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

Limb-girdle muscular dystrophies (NGS panel for 26 genes)

CGC Genetics
Portugal
2626
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 50

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.