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Results: 1 to 20 of 56

Tests names and labsConditionsGenes, analytes, and microbesMethods

MELAS syndrome

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

Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes, MT-CO2 related

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

MELAS syndrome

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

MELAS syndrome

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

Cardiomyopathy, idiopathic dilated, mitochondrial

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

mitochondrial DNA

Laboratory of Biochemistry Caen University Hospital
France
41
  • C Sequence analysis of the entire coding region

Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel

Otogenetics
United States
123129
  • E Sequence analysis of select exons

Mitochondrial Genome Sequencing and Depletion/Integrity Panel

Molecular Genetics Laboratory London Health Sciences Centre
Canada
4752
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Juvenile myopathy, encephalopathy, lactic acidosis AND stroke (MELAS)

Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS
Chile
12
  • T Targeted variant analysis

Mitochondrial Full Genome Analysis

Mayo Clinic Laboratories Mayo Clinic
United States
2937
  • C Sequence analysis of the entire coding region

OtoSCOPE v9

Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics
United States
286218
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PGmito - Mitochondrial Genome Sequencing

PreventionGenetics
United States
1638
  • C Sequence analysis of the entire coding region

mtDNA - mitochondriopathy (MELAS)

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • C Sequence analysis of the entire coding region

mtDNA - mitochondriopathy (encephalopathy)

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • C Sequence analysis of the entire coding region

MELAS m.3243A>G

Inherited Metabolic Disease group University of Cape Town and National Health Laboratory Services
South Africa
21
  • T Targeted variant analysis

MT-TL1. Detection of the mutations m.3243A>G, m.3271T>C and m.3252A>G by sequencing

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

MTTL1. Detection of the mutations m.3243A>G, m.3271T>C and m.3252A>G by sequencing

IGENOMIX
Spain
11
  • T Targeted variant analysis

Melas Syndrome (A3243G)

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • T Targeted variant analysis

Melas Syndrome (A3243G, T3271C, A3252G)

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • T Targeted variant analysis

Melas Syndrome (MTTL1 Gene Sequence Analysis)

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 56

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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