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Results: 1 to 20 of 20

Tests names and labsConditionsGenes and analytesMethods

Glycogen storage disease type XI

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

Metabolic Myopathies, Rhabdomyolysis and Exercise Intolerance Sequencing Panel

PreventionGenetics
United States
7259
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Glycogen Storage Disease and Disorders of Glucose Metabolism Sequencing Panel

PreventionGenetics
United States
2928
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

LDHA Sequence Analysis (Prenatal Diagnosis)

Baylor Miraca Genetics Laboratories
United States
11
  • T Targeted variant analysis

LDHA Sequence Analysis

Baylor Miraca Genetics Laboratories
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

MitoMet®Plus aCGH Analysis

Baylor Miraca Genetics Laboratories
United States
845637
  • D Deletion/duplication analysis

Congenital Myopathy , Panel Massive Sequencing (NGS) 26 Genes

Reference Laboratory Genetics
Spain
2426
  • C Sequence analysis of the entire coding region

Metabolic Myopathy and Rhabdomyolysis

Asper Biogene Asper Biogene LLC
Estonia
5943
  • C Sequence analysis of the entire coding region

Glycogen Storage Disease

Asper Biogene Asper Biogene LLC
Estonia
2525
  • C Sequence analysis of the entire coding region

GLYCOGEN STORAGE: NGS PANEL

Laboratorio de Genetica Clinica SL
Spain
2019
  • C Sequence analysis of the entire coding region

Invitae Comprehensive Glycogen Storage Disease Panel

Invitae
United States
3223
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Muscle Glycogen Storage Disease Panel

Invitae
United States
2014
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NGS Rhabdomyolysis and Metabolic Myopathies Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
4647
  • C Sequence analysis of the entire coding region

NGS Rhabdomyolysis and Metabolic Myopathies Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
4647
  • C Sequence analysis of the entire coding region

METABOLIC MYOPATHIES

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
2325
  • C Sequence analysis of the entire coding region

GLYCOGEN STORAGE DISEASE

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
2424
  • C Sequence analysis of the entire coding region

Metabolic Myopathies Panel

CeGaT GmbH
Germany
2644
  • C Sequence analysis of the entire coding region

Glycogen storage disease type XI (sequence analysis of LDHA gene)

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

LDHA

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
601504
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 20

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