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Results: 21 to 34 of 34

Tests names and labsConditionsGenes, analytes, and microbesMethods

Leukodystrophies , Panel Massive Sequencing (NGS) 57 genes

Reference Laboratory Genetics
Spain
6056
  • C Sequence analysis of the entire coding region

Leukodystrophy and Leukoencephalopathy

Asper Biogene Asper Biogene LLC
Estonia
4739
  • C Sequence analysis of the entire coding region

Autosomal Dominant Adult-Onset Demyelinating Leukodystrophy , Deletions-Duplications (MLPA) LMNB1 Gene

Reference Laboratory Genetics
Spain
11
  • D Deletion/duplication analysis

Leukodistrophy

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
4658
  • C Sequence analysis of the entire coding region

Leukodystrophy, adult-onset, autosomal dominant: LMNB1 gene deletions-duplications analysis (MLPA)

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • D Deletion/duplication analysis

LMNB1 - Del/Dup analysis

Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center
Netherlands
21
  • D Deletion/duplication analysis
  • T Targeted variant analysis

LMNB

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • C Sequence analysis of the entire coding region

Single gene testing LMNB1

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Leukodystrophy / Leukencephalopathy and differential diagnoses Panel

CeGaT GmbH
Germany
69175
  • C Sequence analysis of the entire coding region

LMNB1 Single Gene

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

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Leukoencephalopathy NGS Panel

Fulgent Genetics
United States
15569
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Leukodystrophy, Adult-Onset, Autosomal Dominant

Molecular Diagnostics Lab Nemours Children's Health, Delaware
United States
11
  • D Deletion/duplication analysis

adult-onset autosomal dominant Leukodystrophy

Synlab MVZ Humane Genetik München
Germany
11
  • D Deletion/duplication analysis

Results: 21 to 34 of 34

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.