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Results: 41 to 59 of 59

Tests names and labsConditionsGenes, analytes, and microbesMethods

Single gene testing TREX1

CeGaT GmbH
Germany
41
  • C Sequence analysis of the entire coding region

Aicardi-Goutieres syndrome type 1

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Small vessel disease Panel

CeGaT GmbH
Germany
116
  • C Sequence analysis of the entire coding region

Leukodystrophy / Leukencephalopathy and differential diagnoses Panel

CeGaT GmbH
Germany
69175
  • C Sequence analysis of the entire coding region

Basal ganglia calcification Panel

CeGaT GmbH
Germany
5331
  • C Sequence analysis of the entire coding region

Leukodystrophy and Leukoencephalopathy Panel

CeGaT GmbH
Germany
3635
  • C Sequence analysis of the entire coding region

Leukodystrophy / Leukencephalopathy Panel

CeGaT GmbH
Germany
3635
  • C Sequence analysis of the entire coding region

Aicardi-Goutières Syndrome Panel

CeGaT GmbH
Germany
1010
  • C Sequence analysis of the entire coding region

Epileptic Encephalopathy Panel

CeGaT GmbH
Germany
2577
  • C Sequence analysis of the entire coding region

Aicardi-Goutières Syndrome

MGZ Medical Genetics Center
Germany
16
  • C Sequence analysis of the entire coding region

TREX1 Single Gene

Fulgent Genetics
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

TREX1

MGZ Medical Genetics Center
Germany
31
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51304674
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Leukoencephalopathy NGS Panel

Fulgent Genetics
United States
16970
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Epileptic syndromes with epilepsy and intellectual disability panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
7450
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Aicardi-Goutieres Syndrome NGS Panel

Fulgent Genetics
United States
95
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Eye Disorders NGS Panel

Fulgent Genetics
United States
1018459
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Aicardi-Goutieres syndrome 1

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Test for TREX1-Related Aicardi-Goutieres Syndrome

Secugen SL
Spain
11
  • C Sequence analysis of the entire coding region

Results: 41 to 59 of 59

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.