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Results: 1 to 20 of 22

Tests names and labsConditionsGenes and analytesMethods

Peroxisomal Disorders Sequencing Panel

PreventionGenetics
United States
3222
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

nucSEEK® Comprehensive Sequence Analysis Of The Nuclear Mitochondrial Exome

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
560420
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Peroxisomal disorders

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
3324
  • C Sequence analysis of the entire coding region

Peroxisome biogenesis disorder 2A

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

Zellweger syndrome

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

Zellweger syndrome

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

Lysosomal Storage Disease Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
6574
  • C Sequence analysis of the entire coding region

Single gene testing PEX5

CeGaT GmbH
Germany
21
  • C Sequence analysis of the entire coding region

Peroxisome Biogenesis Disorder panel

Molecular Vision Laboratory
United States
2414
  • C Sequence analysis of the entire coding region

Zellweger syndrome (sequence analysis of PEX5 gene)

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

lysoSEEK™ Sequence Analysis for Lysosomal Storage Disorders

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
11588
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PEX5

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

devACT® Next Generation Sequencing panel focused on genes that inform actionable clinical management of patients with Developmental Delay, Intellectual Disability, and Autism Spectrum Disorders

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
297248
  • L Linkage analysis
  • C Sequence analysis of the entire coding region

Neonatal and Adult Cholestasis: Sequencing Panel

Emory Genetics Laboratory Emory University
United States
9957
  • C Sequence analysis of the entire coding region

Peroxisome Biogenesis Disorders, Zellweger Syndrome Spectrum: Sequencing Panel

Emory Genetics Laboratory Emory University
United States
2414
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

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

Zellweger Syndrome NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
2213
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Peroxisomal NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
3021
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neuromuscular NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
12650
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Lysosomal Disorders NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
193106
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 22

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