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Results: 21 to 30 of 30

Tests names and labsConditionsGenes, analytes, and microbesMethods

Single gene testing PSEN2

CeGaT GmbH
Germany
21
  • C Sequence analysis of the entire coding region

Dementia all Panel

CeGaT GmbH
Germany
3236
  • C Sequence analysis of the entire coding region

Alzheimer's disease Panel

CeGaT GmbH
Germany
811
  • C Sequence analysis of the entire coding region

Frontotemporal Dementia (FTD) Panel

CeGaT GmbH
Germany
2928
  • C Sequence analysis of the entire coding region

PSEN2 Single Gene

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Early Onset Familial Alzheimer Disease (EOFAD) NGS Panel

Fulgent Genetics
United States
93
  • 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

Sudden Death Syndrome NGS Panel

Fulgent Genetics
United States
16868
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Parkinson-Alzheimer-Dementia NGS Panel

Fulgent Genetics
United States
7739
  • 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

Results: 21 to 30 of 30

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.