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Results: 41 to 60 of 76

Tests names and labsConditionsGenes, analytes, and microbesMethods

Spastic paraplegia: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
5554
  • C Sequence analysis of the entire coding region

Childhood Epilepsy NGS Panel

Fulgent Genetics
United States
354209
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neonatal Epilepsy NGS Panel

Fulgent Genetics
United States
509275
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Early-Onset Ataxia NGS Panel

Fulgent Genetics
United States
505132
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pelizaeus-Merzbacher Disease (PLP1 Single Gene Test)

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

Hypomyelinating Leukodystrophy NGS Panel

Fulgent Genetics
United States
22562
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ataxia NGS Panel

Fulgent Genetics
United States
533149
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PLP1-Related Disorders: gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
21
  • C Sequence analysis of the entire coding region

Familial Spastic Paraplegia , Panel Massive Sequencing (NGS) 22 Genes

Reference Laboratory Genetics
Spain
2422
  • C Sequence analysis of the entire coding region

Rett Syndrome and Related Disorders , Panel Massive Sequencing (NGS) 18 Genes

Reference Laboratory Genetics
Spain
1718
  • C Sequence analysis of the entire coding region

Hereditary Spastic Paraplegia NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
8179
  • 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

SPASTIC PARAPLEGIA, FAMILIAL (X-LINKED)

Laboratorio de Genetica Clinica SL
Spain
33
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Familial Spastic Paraplegia Type 2 , Duplication PLP1 Gene

Reference Laboratory Genetics
Spain
11
  • D Deletion/duplication analysis

Familial Spastic Paraplegia Type 2 , Sequencing PLP1 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

HSP, Supplemental Sporadic Evaluation

Athena Diagnostics
United States
2422
  • C Sequence analysis of the entire coding region

HSP, Comprehensive Evaluation

Athena Diagnostics
United States
4024
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HSP, X-Linked Evaluation

Athena Diagnostics
United States
52
  • C Sequence analysis of the entire coding region

Epilepsy Comprehensive NGS Panel

Fulgent Genetics
United States
729398
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PLP1 - Gene Sequencing & Del/Dup analysis

Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center
Netherlands
21
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • T Targeted variant analysis

Results: 41 to 60 of 76

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.