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Results: 1 to 12 of 12

Tests names and labsConditionsGenes and analytesMethods

Familial hemiplegic migraine

Ambry Genetics
United States
44
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Next Generation Sequencing for FHM, EA2, SCA6, CADASIL, Epilepsy

Genomics Research Centre Diagnostics Clinic Queensland Unstitute of Technology
Australia
94
  • C Sequence analysis of the entire coding region

TruGenome Predisposition Screen (Whole Genome Sequencing)

Illumina Clinical Services Laboratory Illumina
United States
15411578
  • C Sequence analysis of the entire coding region

Comprehensive Epilepsy NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
3056447
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Early-Onset Epileptic Encephalopathy NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
1006133
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Idiopathic Generalized Epilepsy NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
106889
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Essential Epilepsy NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
79371
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Migraine Panel

CeGaT GmbH
Germany
510
  • C Sequence analysis of the entire coding region

Familial hemiplegic migraine, episodic ataxia type 2, CACNA1A sequencing

Molecular Diagnostics Laboratory Seoul National University Hospital
South Korea
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Familial Hemiplegic Migraine

Medizinisch Genetisches Zentrum München MGZ München
Germany
15
  • C Sequence analysis of the entire coding region

Familial hemiplegic migraine type 2 (FHM2, deletion/duplication analysis of ATP1A2 gene)

CGC Genetics
Portugal
21
  • D Deletion/duplication analysis

Autism/Intellectual Disability/Multiple Anomalies

Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center
United States
11389
  • C Sequence analysis of the entire coding region

Results: 1 to 12 of 12

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