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Results: 21 to 38 of 38

Tests names and labsConditionsGenes, analytes, and microbesMethods

GPR101 Single Gene

Fulgent Genetics
United States
481
  • D Deletion/duplication analysis
  • 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

Epilepsy

MGZ Medical Genetics Center
Germany
17212
  • C Sequence analysis of the entire coding region

Febrile Seizures

MGZ Medical Genetics Center
Germany
178
  • C Sequence analysis of the entire coding region

Epilepsy and Mitochondrial Encephalopathy

MGZ Medical Genetics Center
Germany
17186
  • C Sequence analysis of the entire coding region

Progressive Myoclonic Epilepsy

MGZ Medical Genetics Center
Germany
1331
  • C Sequence analysis of the entire coding region

Epileptic Encephalopathy – Basic Diagnostics

MGZ Medical Genetics Center
Germany
1422
  • C Sequence analysis of the entire coding region

Malignant Migrating Partial Seizures of Infancy

MGZ Medical Genetics Center
Germany
173
  • C Sequence analysis of the entire coding region

Epileptic Encephalopathy

MGZ Medical Genetics Center
Germany
1789
  • C Sequence analysis of the entire coding region

Familial Focal Epilepsy

MGZ Medical Genetics Center
Germany
86
  • C Sequence analysis of the entire coding region

ESR1 Single Gene

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

EDNRA Single Gene

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

TNF Single Gene

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Juvenile Myoclonic Epilepsy (JME)

MGZ Medical Genetics Center
Germany
172
  • C Sequence analysis of the entire coding region

Malignant Migrating Epilepsy of Infancy

MGZ Medical Genetics Center
Germany
173
  • C Sequence analysis of the entire coding region

Hereditary Hemorrhagic Telangiectasia NGS Panel

Fulgent Genetics
United States
415
  • 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

SCN1A-Related Seizure Disorders

MGZ Medical Genetics Center
Germany
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 38 of 38

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.