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Results: 1 to 17 of 17

Tests names and labsConditionsGenes, analytes, and microbesMethods

Heterotaxy & Situs Inversus Panel, Sequencing

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
736
  • C Sequence analysis of the entire coding region

Syndromal Diseases - panels

MGZ Medical Genetics Center
Germany
14342
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Mental Retardation and Dysmorphology - panels

MGZ Medical Genetics Center
Germany
15343
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neurogenetic Disorders - panels

MGZ Medical Genetics Center
Germany
14597
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Ataxia

Asper Biogene Asper Biogene LLC
Estonia
180139
  • 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

Epilepsy and Hypomyelination

MGZ Medical Genetics Center
Germany
88
  • 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

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

SCN1A-Related Seizure Disorders

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

Results: 1 to 17 of 17

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.