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Results: 1 to 13 of 13

Tests names and labsConditionsGenes, analytes, and microbesMethods

Blepharospasm, primary benign, 606798, Isolated cases (DRD5 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Actionable Epilepsy NGS Panel

Fulgent Genetics
United States
7823
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Dopamine Metabolism Deficiency NGS Panel

Fulgent Genetics
United States
1916
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Progressive Myoclonic Epilepsy NGS Panel

Fulgent Genetics
United States
3617
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Adolescent/Adult Epilepsy NGS Panel

Fulgent Genetics
United States
18282
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neurotransmitter Metabolism Deficiency NGS Panel

Fulgent Genetics
United States
85101
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ADRA2B Single Gene

Fulgent Genetics
United States
171
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HPCA Single Gene

Fulgent Genetics
United States
81
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ANO3 Single Gene

Fulgent Genetics
United States
51
  • 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

DRD5 Single Gene

Fulgent Genetics
United States
21
  • 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

Dystonia Dyskinesia NGS Panel

Fulgent Genetics
United States
6225
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 13 of 13

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.