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Results: 41 to 54 of 54

Tests names and labsConditionsGenes, analytes, and microbesMethods

Benign Familial Neonatal / Infantile Seizures (BFNS/BFIS)

MGZ Medical Genetics Center
Germany
34
  • C Sequence analysis of the entire coding region

Epileptic encephalopathy, early infantile 7, KCNQ2

MVZ Dr. Eberhard & Partner Dortmund
Germany
21
  • C Sequence analysis of the entire coding region

KCNQ2 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

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1103676
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Migraine NGS Panel

Fulgent Genetics
United States
4419
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1058554
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Epileptic encephalopathy panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
5332
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Benign neonatal/infantile convulsions panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
115
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Epilepsy, benign neonatal 1

MedGene
Slovakia
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cardiovascular NGS Panel

Fulgent Genetics
United States
671250
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Arrhythmia NGS Panel

Fulgent Genetics
United States
18476
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Epilepsy, benign neonatal 1

Praxis fuer Humangenetik Wien
Austria
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

KCNQ2

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
11
  • C Sequence analysis of the entire coding region

Results: 41 to 54 of 54

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.